FDA recalls

[GinaMarie]

I get all the FDA recalls on email. I thought I could also post them on here so you can see the most recent recalls. Here is the site with the past recalls in the past 60 days.

http://www.fda.gov/opacom/7alerts.html


If you all want me to keep posting them just let me know. Maybe the moderators can keep it as a sticky post. I also get recalls that ARENT dog/cat food like some on the above link have olives and other things I can post also.
GM

[GinaMarie]

T.W. Enterprises Issues Nationwide Recall of Dog Chews Due to Salmonella Contamination
Contact:
T.W. Enterprises
(360) 366-0408

FOR IMMEDIATE RELEASE -- Ferndale, WA -- April 16, 2007 -- T.W. Enterprises of Ferndale, WA today alerted consumers that it is recalling certain dog chews it markets because they may be contaminated with Salmonella. Samples tested by FDA of the product indicate that the dog chew products manufactured by T.W. Enterprises may be contaminated. People handling these treats can become infected with Salmonella, especially if they have not thoroughly washed their hands after having contact with the chews or any surfaces exposed to these products.

Salmonella can potentially be transferred to people handling these pet treats, especially if they have not thoroughly washed their hands after having contact with the products or any surfaces exposed to these products. Healthy people infected with Salmonella should monitor themselves for some or all of the following symptoms: nausea, vomiting, diarrhea or bloody diarrhea, abdominal cramping and fever. Rarely, Salmonella can result in more serious ailments, including arterial infections, endocarditis, arthritis, muscle pain, eye irritation, and urinary tract symptoms. Consumers exhibiting these signs after having contact with this product should contact their healthcare providers.

Pets with Salmonella infections may be lethargic and have diarrhea or bloody diarrhea, fever, and vomiting. Some pets will have only decreased appetite, fever and abdominal pain. Well animals can be carriers and infect other animals or humans. If your pet has consumed the recalled product and has these symptoms, please contact your veterinarian.

The following is a list of the recalled products (Product Name/ A.B. Dog Chew - Size / UPC):

A.B. Small Chew, 3 - 4 inch / 833234001105
A. B. Puppy Chew, 4 - 6 inch / 83323401112
A.B. Dog Chew Medium, 6 inch / 833234001051
A.B. Dog Chew Large, 10 inch / 833234001068
A. B. Dog Chew XL, 13 inch / 833234001075
A. B. Dog Chew Mega, 16 inch / 833234001082
A. B. Dog Chew Jumbo, 26 inch / 833234001099
T.W. Enterprises Inc. manufactured these dog chews and distributed them throughout the United States under its name. The affected products were distributed before March 22, 2007 to retail locations and are non-coded, i.e. they have no batch code or other identifying marks. T.W. Enterprises has made contact with all of its consignees and has been informed the affected product has been pulled from store shelves.

T.W. Enterprises has informed FDA of its action and is fully cooperating with the agency. The firm, FDA and other authorities are actively investigating this matter to determine the source of this problem, and will take any additional steps necessary to protect the public health. No reports of illness to date in connection with this problem.

Consumers who have the non-coded pet chews should not feed them to their pets, but should dispose of them in a safe manner (e.g., in a securely covered trash receptacle). Anyone who is experiencing the symptoms of Salmonella infection after having handled one of these pet products should seek medical attention, and report their use of the product and illness to the nearest FDA office.

People should thoroughly wash their hands after handling any pet treat – especially those made from animal protein such as meat -- to help prevent infection. People may risk bacterial infection not only by handling the chews, but by contact with pets or surfaces exposed to the chews, so it is important that they thoroughly wash their hands with hot water and soap.

Since elderly people, young children, and people with weakened immune systems are particularly at risk from exposure they should avoid handling these products.

Consumers with questions may contact T.W. Enterprises at 1-360-366-0408.

####



FDA's Recalls, Market Withdrawals and Safety Alerts Page: http://www.fda.gov/opacom/7alerts.html

[GinaMarie]

Recall -- Firm Press Release


FDA posts press releases and other notices of recalls and market withdrawals from the firms involved as a service to consumers, the media, and other interested parties. FDA does not endorse either the product or the company. This listserv covers mainly Class I (life-threatening) recalls. A complete listing of recalls can be found in the FDA Enforcement Report at: http://www.fda.gov/opacom/Enforce.html



Natural Balance Pet Foods, Inc. Issues A Voluntary Nationwide Recall on Specific Venison Dog and Cat Food Products
Contact:
Consumer Inquiries:
(800) 829-4493
Media Inquiries:
Daniel Bernstein
310-275-0777

FOR IMMEDIATE RELEASE -- Pacoima, CA -- April 17, 2007 -- Natural Balance, Pacoima, CA, is issuing a voluntary nationwide recall for all of its Venison dog products and the dry Venison cat food only, regardless of date codes. The recalled products include Venison and Brown Rice canned and bagged dog foods, Venison and Brown Rice dog treats, and Venison and Green Pea dry cat food. Recent laboratory results show that the products contain melamine. We believe the source of the melamine is a rice protein concentrate. Natural Balance has confirmed this morning that some production batches of these products may contain melamine.

The recall was prompted by consumer complaints received by Natural Balance involving a small number of cats and dogs that developed kidney failure after eating the affected product.

Dogs or cats who have consumed the suspect food and show signs of kidney failure (such as loss of appetite, lethargy and vomiting) should be seen by a veterinarian. We recommend our customers immediately stop feeding our recalled venison products regardless of date code and return unused product to their retailer for a full refund.

The products are packaged in bags, cans and zip lock treat bags and sold in pet specialty stores and PetCo nationally.

No other Natural Balance products are involved in this voluntary recall as none of our other formulas include the rice protein concentrate.

Although the problems seem to be focused on a particular production period of the venison products, over the last four days we have notified our distributors and retailers by phone and e-mail to immediately stop selling and return all recalled Venison dog foods and treats and the Venison dry cat food. Venison canned cat food is not involved.

The source of the melamine appears to be a rice protein concentrate, which was recently added to the dry venison formulas. Natural Balance does not use wheat gluten, which was associated with the previous melamine contamination.

None of Natural Balance's other dry formulas, none of our other canned or roll products and none of our other treats are involved with this voluntary recall.

We continue to work closely with the FDA in their ongoing investigation.

Consumers with questions may contact the company at 1-800-829-4493 or visit the website at www.naturalbalance.net.

####

FDA's Recalls, Market Withdrawals and Safety Alerts Page: http://www.fda.gov/opacom/7alerts.html

[GinaMarie]

Recall -- Firm Press Release


FDA posts press releases and other notices of recalls and market withdrawals from the firms involved as a service to consumers, the media, and other interested parties. FDA does not endorse either the product or the company. This listserv covers mainly Class I (life-threatening) recalls. A complete listing of recalls can be found in the FDA Enforcement Report at: http://www.fda.gov/opacom/Enforce.html



Jen-On Herbal Science International, Inc. Issues A Voluntary Nationwide Recall of H S Joy of Love, a Product Marketed as a Dietary Supplement
Contact:
Dr. William Chang
(626) 333-9998

FOR IMMEDIATE RELEASE -- City of Industry, CA -- April 17, 2007- Jen-On Herbal Science International, Inc. 205 Russell St., City of Industry, CA 91744, announced today that it is conducting a voluntary nationwide recall of the company's supplement product sold under the name H S Joy of Love. Jen-On Herbal Science International, Inc. is conducting this recall after being informed by representatives of the Food and Drug Administration (FDA) that lab analysis by FDA of H S Joy of Love samples found the product contains Piperadino Vardenafil, an analog of Vardenafil, an FDA-approved drug used as treatment for male Erectile Dysfunction (ED). Piperadino Vardenafil is close in structure to Vardenafil and is expected to possess a similar pharmacological and adverse event profile. This poses a threat to consumers because the analogue may interact with nitrates found in some prescription drugs (such as nitroglycerin) and may lower blood pressure to dangerous levels. Consumers with diabetes, high blood pressure, high cholesterol, or heart disease often take nitrates. ED is a common problem in men with these conditions, and consumers may seek these types of products to enhance sexual performance.

H S Joy of Love is sold nationwide. The H S Joy of Love product is sold as a 12-capsule blister pack packaged in a retail box.

Consumers who have H S Joy of Love in their possession should stop using it immediately. In the event of any adverse side effects due to its consumption, consumers should contact a physician right away. Any adverse events that may be related to the use of this product should be reported to the FDA's MedWatch Program by phone at 1-800-FDA-1088 or by fax at 1-800-FDA-0178 or by mail at MedWatch, HF-2, FDA, 5600 Fishers Lane, Rockville, MD 20852-9787.

The company advises that any unused portion be returned to Jen-On Herbal Science International, Inc. for a full purchase price refund by calling (626) 333-9998 for instructions on the return and refund process.

No illnesses have been reported to the company to date in connection with this product.

Jen-On Herbal Science International, Inc. apologizes for any inconvenience and expresses its concerns for the health of consumers by conducting a voluntary recall action. Jen-On Herbal Science International, Inc. promises to ensure quality and integrity of all its products and the company is working closely with the FDA in the recall process.

####



FDA's Recalls, Market Withdrawals and Safety Alerts Page: http://www.fda.gov/opacom/7alerts.html

[GinaMarie]

Recall -- State Press Release



This listserv covers mainly Class I (life-threatening) recalls. A complete listing of recalls can be found in the FDA Enforcement Report at: http://www.fda.gov/opacom/Enforce.html

Agriculture Department Warns Consumers of Tainted Raw Milk Sold by Butler County Dairy

Contact:
Chris L. Ryder
(717) 503-0035 (cell)

FOR IMMEDIATE RELEASE -- Harrisburg, PA -- April 13, 2007 -- Consumers who have purchased raw milk from Fisher's Dairy, Butler County, any time after April 9, 2007, should discard it immediately due to the risk of Listeria monocytogenes contamination, Agriculture Secretary Dennis Wolff said today.

"During routine inspection, a preliminary test showed the presence of Listeria bacteria in some of the raw milk samples taken from Fisher's Dairy," said Wolff. "If consumers have raw milk from this farm, they should discard it immediately."

There have been no illnesses reported because of the potential contamination, but if individuals who consumed the raw milk become ill, they are advised to consult their physician.

Raw milk is milk that has not been pasteurized or homogenized.

The Department of Agriculture has suspended sales of raw milk at the dairy and is ensuring that corrective action is taken. Samples taken from the farm during routine testing on April 9 tested positive for Listeria on April 13.

Multiple laboratory samples must come back negative before sales can resume.

Symptoms of Listeriosis are fever, muscle aches, and sometimes gastrointestinal symptoms such as nausea or diarrhea. If infection spreads to the nervous system, symptoms such as headache, stiff neck, confusion, loss of balance or convulsions can occur.

Infected pregnant women may experience only a mild, flu-like illness, but infections during pregnancy can lead to miscarriage or stillbirth.

Symptoms of Listeriosis can appear in four days to three weeks.

####

FDA's Recalls, Market Withdrawals and Safety Alerts Page: http://www.fda.gov/opacom/7alerts.html

[GinaMarie]

Recall -- Firm Press Release


FDA posts press releases and other notices of recalls and market withdrawals from the firms involved as a service to consumers, the media, and other interested parties. FDA does not endorse either the product or the company. This listserv covers mainly Class I (life-threatening) recalls. A complete listing of recalls can be found in the FDA Enforcement Report at: http://www.fda.gov/opacom/Enforce.html



Wilbur-Ellis Voluntarily Recalls Rice Protein Concentrate
Contact:
Ann Barlow
415-438-9826; 925-200-6539
Deborah Brown
212-931-6113

FOR IMMEDIATE RELEASE -- San Francisco, CA -- April 18, 2007 -- Wilbur-Ellis Company is voluntarily recalling all lots of the rice protein concentrate the San Francisco company’s Feed Division has shipped to pet-food manufacturers because of a risk that rice protein concentrate may have been contaminated by melamine, an industrial chemical used to make plastics and fertilizers that can lead to illness or fatalities in animals if consumed.

Wilbur-Ellis noted that it obtained rice protein from a single source in China and shipped to a total of five U.S. pet-food manufacturers located in Utah, N.Y., Kansas and two in Missouri.

Last Sunday, April 15, Wilbur-Ellis notified the U.S. Food and Drug Administration that a single bag in a recent shipment of rice protein concentrate from its Chinese supplier, Binzhou Futian Biology Technology Co. Ltd., had tested positive for melamine. Unlike the other white-colored bags in that shipment, the bag in question was pink and had the word “melamine” stenciled upon it. Wilbur-Ellis separated that bag and quarantined the entire shipment for further testing and since that time, no further deliveries of rice protein concentrate have been made. Samples from the white bags tested negative for melamine. However, subsequent and potentially more sensitive tests by the FDA came back positive for melamine, leading Wilbur-Ellis to voluntarily issue the recall.

Wilbur-Ellis began importing rice protein concentrate from Binzhou Futian Biology Technology in July 2006. A total of 14 containers holding 336 metric tons of rice protein concentrate were sent from Futian to Wilbur-Ellis. Wilbur-Ellis has distributed 155 metric tons to date.

On Monday (April 16), a pet food distributor issued a voluntary recall of its pet food, believing the source of contamination to be rice protein concentrate supplied by Wilbur-Ellis. As an additional precaution, Wilbur-Ellis is urging all pet food manufacturers using rice protein concentrate supplied through Wilbur-Ellis to recall any pet food that may be on supermarket shelves.

Consumers with questions about the pet food they use should visit the FDA Web site at www.fda.gov.

####

FDA's Recalls, Market Withdrawals and Safety Alerts Page: http://www.fda.gov/opacom/7alerts.html

[GinaMarie]

Recall -- Firm Press Release


FDA posts press releases and other notices of recalls and market withdrawals from the firms involved as a service to consumers, the media, and other interested parties. FDA does not endorse either the product or the company. This listserv covers mainly Class I (life-threatening) recalls. A complete listing of recalls can be found in the FDA Enforcement Report at: http://www.fda.gov/opacom/Enforce.html



Royal Canin USA Announces the Voluntary Nationwide Recall of its Dry Pet Food Products Containing Rice Protein Concentrate

Contact:
Erik Mueller
636-926-1089

FOR IMMEDIATE RELEASE -- St Charles, Missouri -- April 19, 2007 -- Royal Canin USA is announcing today that the company has determined there is a melamine derivative in the rice protein concentrate in some of its dry pet food products.

Although Royal Canin USA has no confirmed cases of illness in pets, we have decided to voluntarily remove all of our dry pet food products containing rice protein concentrate. We are taking this proactive stance to avoid any confusion for our customers about which Royal Canin USA products are safe and which products may be affected.

"We are as passionate about the health and happiness of our customers' pets as we are of our own, so we are committed to taking the steps necessary to ensure this never happens again," said Olivier Amice, President and CEO of Royal Canin USA.

As a precaution, Royal Canin USA is voluntarily recalling the following dry pet food products:

ROYAL CANIN VETERINARY DIET™ (available only in veterinary clinics)
Dry Dog Food

Canine Early Cardiac EC 22™
Canine Skin Support SS21™
Dry Cat Food

Feline Hypoallergenic HP23™
ROYAL CANIN SENSIBLE CHOICE® (available in pet specialty stores nationwide)

Dry Dog Food

Chicken Meal & Rice Formula Senior
Lamb Meal & Rice Formula Puppy
Lamb Meal & Rice Formula Adult
Lamb Meal & Rice Formula Senior
Rice & Catfish Meal Formula Adult
Based on today's announcement, pet owners should immediately stop feeding their pets the Royal Canin USA dry pet food products listed above. Pet owners should consult with a veterinarian if they are concerned about the health of their pet. No other Royal Canin diets are affected by this recall and CONTINUE TO BE safe for pets to eat.

Along with this announcement, Royal Canin USA will no longer use any Chinese suppliers for any of our vegetable proteins.

"On behalf of the entire Royal Canin family, our hearts go out to the pet owners and everyone in the pet community who have been affected by all of the recent recalls," said Dr. Denise Elliott, Director of Scientific Affairs for Royal Canin USA. "We are working very closely with the FDA to assist in its efforts to determine the cause of this most recent and disturbing development."

The safety and nutritional quality of our pet food is Royal Canin USA's top priority as we understand that the health of pets comes first. Pet owners who have questions about this recall and other Royal Canin USA products should call 1-800-592-6687 or visit our web site at www.royalcanin.us.

All Royal Canin USA products have a satisfaction guarantee and we will refund or replace the diets that have been recalled.

####



FDA's Recalls, Market Withdrawals and Safety Alerts Page: http://www.fda.gov/opacom/7alerts.html

[GinaMarie]

Recall -- Firm Press Release


FDA posts press releases and other notices of recalls and market withdrawals from the firms involved as a service to consumers, the media, and other interested parties. FDA does not endorse either the product or the company. This listserv covers mainly Class I (life-threatening) recalls. A complete listing of recalls can be found in the FDA Enforcement Report at: http://www.fda.gov/opacom/Enforce.html



Blue Buffalo Company Announces Voluntary Recall of One Production Run of Spa Select Kitten Dry Food

Contact:
Consumer Inquiries:
1-800-919-2833
Media Inquiries:
David Petrie
1-203-762-9751

FOR IMMEDIATE RELEASE -- Wilton, Connecticut, April 19, 2007 -- The Blue Buffalo Company today announced a voluntary recall of one production run of its Spa Select Kitten dry food.

The recalled 3 lb. and 7 lb. bags of Spa Select Kitten dry food have the production code "BEST IF USED BY MAR 07 08 B" printed on the bag. Consumers should check this information on the bag, which is printed on the back panel below the seal.

The Company has taken this action because the rice protein concentrate used for this particular production run was obtained from Wilbur-Ellis, the same company who supplied this ingredient to Natural Balance. Test results received the evening of April 18th indicated that this rice protein concentrate tested positive for melamine. This was the only production run that used rice protein from Wilbur-Ellis.

Upon receiving the test results, the Company notified the FDA today and immediately began this recall process.

Of the 5,044 bags produced in this particular production run, the Company was able to prevent the majority from ever entering retail distribution. The Company is working closely with its retail partners and believes that most of the recalled product that had reached retail distribution has already been pulled off the shelf.

Consumers should immediately stop feeding Spa Select Kitten dry cat food with the above-listed date codes to their kittens and consult with a veterinarian if they have any health concerns with their pet.

No other cat or dog foods, canned or dry, made by the Company are affected by the recall.

Should consumers have a specific question, they can email the Company at info@bluebuff.com or call 1-800-919-2833, Monday through Friday, 9 a.m. to 5 p.m. EDT, to receive more information.

Bill Bishop, CEO and President of The Blue Buffalo Company, commented "As a family owned company whose reason for being is to provide cats and dogs with the highest quality natural foods, we are extremely upset by this recall and can't begin to apologize enough to our customers. From our perspective, it is unacceptable to produce even one bag of food with the potential to cause a pet to become ill, and we will further tighten our ingredient sourcing and quality assurance procedures as a result of this incident."

####

FDA's Recalls, Market Withdrawals and Safety Alerts Page: http://www.fda.gov/opacom/7alerts.html

[GinaMarie]

Recall -- Firm Press Release


FDA posts press releases and other notices of recalls and market withdrawals from the firms involved as a service to consumers, the media, and other interested parties. FDA does not endorse either the product or the company. This listserv covers mainly Class I (life-threatening) recalls. A complete listing of recalls can be found in the FDA Enforcement Report at: http://www.fda.gov/opacom/Enforce.html



ResMed Issues a Voluntary Recall for Certain 58 Flow Generators

Contact:
Hillary Theakston
858-746-2610

FOR IMMEDIATE RELEASE -- San Diego, CA, April 23, 2007 — ResMed today announced a worldwide voluntary recall of approximately 300,000 of its early production S8 flow generators used for the treatment of obstructive sleep apnea. In S8 devices manufactured between July 2004 and May 15, 2006, there is a remote potential for a short circuit in the power supply connector. ResMed plans to work with its distribution partners globally to provide a replacement device to patients who have an affected S8 flow generator.

Patients may continue to use their S8 flow generators until they receive a replacement device. As with any electrical device, patients should make sure that it is placed on a hard clean surface and that the area around the device is clear during use. Patients should discontinue use of the device if there are any signs of electrical failure such as intermittent power, cracking sounds, sparking or charred smell. Patients should not use supplemental oxygen with an affected device; patients using supplemental oxygen should immediately contact their home healthcare provider for a replacement.

The recall includes the following serial number ranges for all S8 models:

From
To

20040285613
20060269563

20060275728
20060276751

20060277160
20060277415

20060281672
20060281991

20060283424
20060283743

20060284896
20060285445

20060287568
20060290823

20060292360
20060294694

20060312361
20060312597

20060318692
20060319459

20060325074
20060327794

20060330588
20060331043



ResMed voluntarily recalled the product after learning that in rare instances — less than two tenths of one percent (0.2%) — a short circuit in the power supply connector, a component supplied by a third party, has caused the devices to fail. In only seven cases worldwide, device failures have led to thermal damage to the device, with a remote potential to ignite material external to the device. No significant property damage or patient injury has been reported.

ResMed has advised the U.S. Food and Drug Administration and other regulatory authorities of this action. ResMed is continuing to discuss this action with those authorities and will finalize its proposed course of action after those discussions are concluded.

ResMed's S8 flow generators are distributed through medical equipment suppliers throughout the world. Affected products can be identified by the serial numbers on the bottom of each device. ResMed is working in close partnership with its distribution partners and the medical community to ensure that patients are fully aware of the replacement program and that patients who have an affected device will receive a replacement S8 flow generator.

Patients will be contacted as soon as possible to arrange for a replacement device and are encouraged to visit http://www.resmed.com/en-us/s8program/s8program.html for more information. Patients in the U.S. and Canada may also contact the ResMed S8 Replacement Call Center at 888-899-8991. Contact information for patients in Latin America, Europe and Asia Pacific is available at www.resmed.com/s8program.

Adverse reactions or quality problems experienced with the use of this product may be reported to the FDA's Med Watch Adverse Event Reporting Program either online, by regular mail or by fax.

Online: www.fda.gov/medwatch/report.htm
Regular mail: Use postage-paid FDA form 3500 available at:
www.fda.gov/medwatch/getforms.htm. Mail to: MedWatch 5600 Fishers Lane, Rockville, MD 20852-9787
Fax: 1-800-FDA-0 178
####

FDA's Recalls, Market Withdrawals and Safety Alerts Page: http://www.fda.gov/opacom/7alerts.html

__________________________________________________ _



Thanks for subscribing to the FDA Recalls list.



To subscribe to or unsubscribe from this list, go to

https://list.nih.gov/archives/fda-recalls-l.html

[GinaMarie]

Recall -- Firm Press Release


FDA posts press releases and other notices of recalls and market withdrawals from the firms involved as a service to consumers, the media, and other interested parties. FDA does not endorse either the product or the company. This listserv covers mainly Class I (life-threatening) recalls. A complete listing of recalls can be found in the FDA Enforcement Report at: http://www.fda.gov/opacom/Enforce.html



LiveSmart Weight Management Chicken and Brown Rice Recall
Contact:
SmartPak
1-800-326-0282

STATEMENT: On Friday, April 20, SmartPak initiated a voluntary recall of a single production run of the LiveSmart Weight Management Chicken and Brown Rice Dog Food.

The particular lot of food recalled included rice protein concentrate that was supplied by Wilbur-Ellis, the same company that supplied rice protein concentrate contaminated with Melamine to Natural Balance. This was the first time that our supplier purchased and used rice protein concentrate from Wilbur-Ellis. No previous lots were affected, nor do we use rice protein concentrate in any other formulas of LiveSmart dog or cat foods.

Thankfully, the product was just produced, and only a very limited amount of product had left our facility prior to the recall (less than 1200 pounds). We have notified every affected pet owner via both phone and email.

We have not had any reports of injury to any dogs. Dogs who have consumed the LiveSmart Weight Management food and show signs of kidney failure (such as loss of appetite, lethargy and vomiting) should be seen by a veterinarian.

We have temporarily suspended further distribution of the LiveSmart Weight Management Chicken and Brown Rice Dog Food. We will notify you when we have the product back in stock and will continue to update our website as more information becomes available.

####

FDA's Recalls, Market Withdrawals and Safety Alerts Page: http://www.fda.gov/opacom/7alerts.html

__________________________________________________ _



Thanks for subscribing to the FDA Recalls list.



To subscribe to or unsubscribe from this list, go to

https://list.nih.gov/archives/fda-recalls-l.html

[GinaMarie]

Recall -- Firm Press Release


FDA posts press releases and other notices of recalls and market withdrawals from the firms involved as a service to consumers, the media, and other interested parties. FDA does not endorse either the product or the company. This listserv covers mainly Class I (life-threatening) recalls. A complete listing of recalls can be found in the FDA Enforcement Report at: http://www.fda.gov/opacom/Enforce.html



Chenango Valley Pet Foods Issues Voluntarily Nationwide Recall of Certain Pet Foods

Contact:
Dennis J. Bobita
(610) 821-0608

FOR IMMEDIATE RELEASE -- April 26, 2007 -- Chenango Valley Pet Foods is working with the U.S. Food and Drug Administration and voluntarily recalling pet foods manufactured with a certain shipment of rice protein concentrate. The company was informed by Wilbur-Ellis that the rice protein concentrate shipped to Chenango Valley Pet Foods may be contaminated with melamine, and instructed Chenango Valley Pet Foods to recall any pet foods manufactured with the rice protein concentrate. Melamine is an industrial chemical used to make plastics and fertilizers that may lead to illness or fatalities in animals if consumed.

The pet foods were sold to customers in Wisconsin, Massachusetts, and Pennsylvania, who further sold the products to their customers through catalog mail-orders or retail outlets.

Only the following dry pet foods are involved in the recall:

DOCTORS FOSTER & SMITH CHICKEN & BROWN RICE FORMULA ADULT LITE DOG FOOD, NET WT. 5 LBS., 12.5 LBS, and 25 LBS; Code dates: Best Used By Jan 24, 09; Best Used By Feb 8, 09; Best Used By Feb 26, 09; Best Used By April 10, 09; Best Used By April 17, 09;

DOCTORS FOSTER & SMITH CHICKEN & BROWN RICE FORMULA ADULT LITE CAT FOOD, NET WT. 3 LBS. and 7 LBS.; Code date: Best Used By March 13, 09;

LICK YOUR CHOPS LAMB MEAL, RICE & EGG CAT FOOD, 4 LBS. packages,
Code date: Best Used By April 29, 08;

Bulk CHICKEN & BROWN RICE FORMULA ADULT LITE DOG FOOD sold to one consignee (SmartPak) in a 2000 lbs. tote, Ship date: Feb 9, 2007.

No illnesses or injuries have been reported to date.

Pet owners who purchased the pet foods should immediately discontinue using the products and return them to the place of purchase for a full refund. Pet owners should consult with a veterinarian if they have any health concerns with their pet. Consumers with questions may contact the company at 1-610-821-0608.

####

FDA's Recalls, Market Withdrawals and Safety Alerts Page: http://www.fda.gov/opacom/7alerts.html

[RathyKay]

I had to buy dog food today. Our brand still hasn't had a recall, but I keep wondering. Anyway, thanks for posting this. I do check your updates.

[Mom2Ava]

My Kittys have been effectd by this :( . It has been getting very expensive.
Our new vet says at this point she really recommends the home prepared diets.

[GinaMarie]

Recall -- Firm Press Release


FDA posts press releases and other notices of recalls and market withdrawals from the firms involved as a service to consumers, the media, and other interested parties. FDA does not endorse either the product or the company. This listserv covers mainly Class I (life-threatening) recalls. A complete listing of recalls can be found in the FDA Enforcement Report at: http://www.fda.gov/opacom/Enforce.html

Diamond Pet Food Withdraws Products in Response to American Nutrition Inc. Pet Food Recall

Contact:
Diamond Pet Food Media Hotline
(888) 207-6208

FOR IMMEDIATE RELEASE -- Meta, MO -- April 26, 2007 -- Because of the canned pet food recall initiated today by American Nutrition Inc., Diamond Pet Foods has announced it is withdrawing a limited number of canned products manufactured by American Nutrition. This action is limited to three specific canned products: Diamond Lamb & Rice Formula for Dogs 13 oz. cans, Chicken Soup for the Pet Lover's Soul Kitten Formula 5.5 oz. cans, and Chicken Soup for the Pet Lover's Soul Puppy Formula 13 oz. cans.

Diamond Pet Foods is taking this voluntary action after learning the Food and Drug Administration (FDA) confirmed rice protein concentrate used by American Nutrition contained melamine, a substance not approved for use in food.

No other Diamond brand or Chicken Soup brand canned or dry pet food formulas are affected by the American Nutrition recall.

Diamond Pet Foods has not received any indication of quality or safety issues, including pet illness, with the three withdrawn products. However, because American Nutrition informed the company that these three specific products may include rice protein concentrate, Diamond Pet Foods felt this action was necessary for the protection of its customers and their pets.

It should be noted that the products being withdrawn were not formulated or labeled to contain rice protein concentrate. While the FDA is investigating this, current information indicates this error is a result of a manufacturing deviation by American Nutrition.

####

FDA's Recalls, Market Withdrawals and Safety Alerts Page: http://www.fda.gov/opacom/7alerts.html

[GinaMarie]

Recall -- Firm Press Release


FDA posts press releases and other notices of recalls and market withdrawals from the firms involved as a service to consumers, the media, and other interested parties. FDA does not endorse either the product or the company. This listserv covers mainly Class I (life-threatening) recalls. A complete listing of recalls can be found in the FDA Enforcement Report at: http://www.fda.gov/opacom/Enforce.html



Blue Buffalo Recalls Can and Biscuit Products Due To Tampering By American Nutrition Inc.
Contact:
Consumer Inquiries:
1-800-919-2833
Media Inquiries:
David Petrie
1-203-762-9751

FOR IMMEDIATE RELEASE -- Wilton, Connecticut, April 26, 2007- We at the Blue Buffalo Company have just learned that American Nutrition Inc. (ANI), the manufacturer of all our cans and biscuits, has been adding rice protein concentrate to our can formulas without our knowledge and without our approval. This is product tampering, and it apparently has been going on for some time. The can formulas that we developed, and trusted them to produce, never contained any rice protein concentrate. It appears that only an FDA investigation of ANI's rice protein concentrate supplies forced them to reveal this product tampering to us.

While this activity by ANI is in itself unlawful, the situation is further clouded by the fact that ANI has been receiving rice protein concentrate from Wilber-Ellis, some of which the FDA has determined to be contaminated with melamine.

So while no BLUE or Spa Select canned product has tested positive for the presence of melamine, and there has been no reported illness due to any of our canned products, we simply cannot be sure of what ANI has been including in our formulas. For this reason, we have decided to remove all of our canned and biscuit products from retail distribution. While this may seem to many to be a major over-reaction, as other ANI customers will probably only recall the products that tested positive for melamine, we see this as a matter of integrity.

We founded Blue Buffalo on the principle of providing dogs and cats with the highest quality and most nutritious food, and we will not sell any product that doesn't meet this standard. And under these circumstances, we cannot say that any products manufactured by ANI measure up.

The obvious question is "how could Blue Buffalo not know that ANI was putting rice protein concentrate into our canned food?" The answer is we trusted them. In business and in life, we all trust our partners to deal with us honestly. When we buy produce from our local grocery store, we are trusting growers, shippers and a series of handlers to have delivered a product that is safe and nutritious for our family. If any one of these parties betrays our trust, contaminated products can make their way to our dinner table.

And while we test for known toxins and contaminants, we don't test for protein sources, like rice protein concentrate, especially when we did not formulate our products to contain them.

In the end, this all comes down to an issue of integrity, and ANI has not been honest with us and with the pet parents who buy our products. We will not put any product made by ANI on the shelf, and are temporarily withdrawing an important part of our business in order to be true to our pet parents.

We have already started the process of identifying a can and biscuit manufacturer with whom we can build a partnership based on trust. Once we have accomplished this, BLUE and Spa Select cans and BLUE Health Bars will be reintroduced with the high quality and superior nutrition that our brand stands for and that dogs and cats deserve.

We have informed our retail partners and the FDA about this action and will be cooperating with them to complete this recall quickly. The specific product involved includes all "BLUE" brand can dog foods, all "Spa Select" brand can cat foods and all "BLUE Health Bar" treats.
Consumers who have unused or partially used packages of any of these products should return them to their place of purchase for a complete refund.

All "BLUE" dry natural food for dogs and "Spa Select" dry natural foods for cats are not affected by this recall and are safe for consumption. Should consumers have a specific question, they can call the Company at 1-800-919-2833, Monday through Friday, 9 a.m. to 5 p.m. EDT, to receive more information.

####

FDA's Recalls, Market Withdrawals and Safety Alerts Page: http://www.fda.gov/opacom/7alerts.html

[GinaMarie]

Recall -- Firm Press Release


FDA posts press releases and other notices of recalls and market withdrawals from the firms involved as a service to consumers, the media, and other interested parties. FDA does not endorse either the product or the company. This listserv covers mainly Class I (life-threatening) recalls. A complete listing of recalls can be found in the FDA Enforcement Report at: http://www.fda.gov/opacom/Enforce.html



American Nutrition, Inc. Issues Voluntary Recall

Contact:
Bill Behnken, 801.394.3477, bill@amnutrition.com
Naomi Keller, 801.554.0023, naomi@amnutrition.com

FOR IMMEDIATE RELEASE -- April 26, 2007 -- The Denver office of the FDA informed American Nutrition, Inc. today that certain samples of rice protein shipped to its production facility have been contaminated with melamine, an industrial chemical used to make plastics and fertilizers that may be harmful to animals if consumed. The rice protein in question was obtained from San Francisco-based Wilbur-Ellis Company.

The FDA is investigating the use of rice protein, an ingredient found in a number of canned pet food products and baked pet food treats to fortify protein levels, after a portion of Wilbur-Ellis' rice protein supply was found to be contaminated with melamine. American Nutrition immediately discontinued the use of rice protein after learning of the melamine contamination.

The FDA has urged American Nutrition to issue a voluntary recall of pet foods manufactured using Wilbur-Ellis rice protein. None of these products is sold under an American Nutrition brand, but are sold through other independent companies. No American Nutrition brands or other products they manufacture for other businesses are affected by this recall.
The products subject to this recall are as follows:

CANNED CAT FOOD
Blue Buffalo Spa Select Hairball Control Oven Roasted Chicken 3oz AUG 21 09 APR 15 10
Blue Buffalo Spa Select Kitten Recipe Oven Roasted Chicken 3oz AUG 21 09 APR 15 10
Chicken Soup for the Pet Lover's Soul Kitten Formula 5.5oz 15 AUG 08 15 APR 09
Harmony Farms Country Chicken Entrée 3oz AUG 21 09 APR 15 10
Natural Balance Ocean Fish Formula 3oz and 6 oz AUG 21 09 APR 15 10

CANNED DOG FOOD
Blue Buffalo Beef Dinner 12.5oz AUG 21 09 APR 15 10
Blue Buffalo Chicken Dinner 12.5oz AUG 21 09 APR 15 10
Blue Buffalo Hearty Venison Dinner 12.5oz AUG 21 09 APR 15 10
Blue Buffalo Lamb Dinner 12.5oz AUG 21 09 APR 15 10
Blue Buffalo Salmon Dinner 12.5oz AUG 21 09 APR 15 10
Blue Buffalo Turkey Meatloaf Dinner 12.5oz AUG 21 09 APR 15 10
Canine Caviar Gourmet Beaver 13.2oz AUG 21 08 APR 15 09
Canine Caviar Gourmet Turkey 13.2oz AUG 21 08 APR 15 09
Chicken Soup for the Pet Lover's Soul Puppy Formula 13oz 21 AUG 08 15 APR 09
Diamond Lamb & Rice 13oz 21 AUG 09 15 APR 10
Harmony Farms Beef 12.5oz AUG 21 09 APR 15 10
Harmony Farms Chicken 12.5oz AUG 21 09 APR 15 10
Harmony Farms Lamb 12.5oz AUG 21 09 APR 15 10
Harmony Farms Salmon 12.5oz AUG 21 09 APR 15 10
Kirkland Signature Premium Dog 2-Flavor Variety Pack 14oz (24-pack) AUG 21 08 APR 15 09
Mulligan Stew Chicken 13.2oz AUG 21 09 APR 15 10
Mulligan Stew Turkey 13.2oz AUG 21 09 APR 15 10
Natural Balance Beef Formula 13oz AUG 21 09 APR 15 10
Natural Balance Chicken Formula 13oz AUG 21 09 APR 15 10
Natural Balance Lamb Formula 13oz AUG 21 09 APR 15 10
Natural Balance Venison & Brown Rice 13oz AUG 21 09 APR 15 10

BAKED DOG TREATS
Natural Balance Venison & Brown Rice Formula Baked Dog Treats 14oz AUG 21 07 APR 15 08
Blue Buffalo Health Bars Baked With Apples & Yogurt Dog Treats 20oz AUG 21 07 APR 15 08

Pet owners who purchased these pet foods should immediately discontinue using the products and return unused portions to the place of purchase for a full refund.

These products represent a small percentage of those manufactured by American Nutrition. To reiterate, no American Nutrition brands or other products manufactured for other businesses are affected by this recall.

We at American Nutrition care immensely about the quality of the products we manufacture and the health of the pets that consume them. We want to express our deep concern over this situation. Feeding pets has been our business and passion for more than 35 years. We take that responsibility seriously and are very proud of what we do and how we do it. We will continue to work closely with the FDA in their ongoing investigation.

For more information, we encourage you to visit the FDA website: www.fda.gov. Consumers with additional questions can contact us by calling 1.800.257.4530 or by e:mailing us at feedback@amnutrition.com or by visiting www.americannutritioninc.com.

####

FDA's Recalls, Market Withdrawals and Safety Alerts Page: http://www.fda.gov/opacom/7alerts.html

[GinaMarie]

There are so many I have gotten in the past few days Im putting at least two recalls in one post so make sure you read all of them. SOME are NOT dog/cat food related. They are medical or human food related..


Recall -- Firm Press Release


FDA posts press releases and other notices of recalls and market withdrawals from the firms involved as a service to consumers, the media, and other interested parties. FDA does not endorse either the product or the company. This listserv covers mainly Class I (life-threatening) recalls. A complete listing of recalls can be found in the FDA Enforcement Report at: http://www.fda.gov/opacom/Enforce.html



Natural Balance Pet Foods, Inc. Recalls Products in Response to American Nutrition Inc. Pet Food Recall
Contact:
Natural Balance Consumer Contact:
1-800-829-4493

FOR IMMEDIATE RELEASE -- Pacoima, CA -- April 27, 2007 -- Because of the pet food recall initiated today by American Nutrition Inc., Natural Balance Pet Foods has announced it is issuing a nationwide recall of a number of canned products manufactured by American Nutrition. This action is limited to four specific Natural Balance canned formulas: Chicken Canned Dog Formula 13 oz , Beef Canned Dog Formula 13 oz, Lamb Canned Dog Formula 13 oz, and the 3oz and 6 oz Ocean Fish Canned Cat Formulas.

Natural Balance Pet Foods is taking this voluntary action after learning the Food and Drug Administration (FDA) confirmed rice protein concentrate used by American Nutrition contained melamine, a substance not approved for use in food. These products are being recalled in addition to our previously recalled Venison and Brown Rice canned and bagged dog foods, Venison and Brown Rice dog treats, and Venison and Green Pea dry cat food.

Natural Balance Pet Foods has not received any indication of quality or safety issues, including pet illness, with the four withdrawn formulas. However, because American Nutrition informed the company that these four specific products may include rice protein concentrate, Natural Balance Pet Foods felt this action was necessary for the protection of its customers and their pets.

It should be noted that the products being recalled were not formulated or labeled to contain rice protein concentrate. While the FDA is investigating this, current information indicates this error is a result of a manufacturing deviation by American Nutrition. Natural Balance is working with the FDA in this matter.

####

FDA's Recalls, Market Withdrawals and Safety Alerts Page: http://www.fda.gov/opacom/7alerts.html

`````````````````````````````````````````````````` ``````````````

Recall -- Firm Press Release


FDA posts press releases and other notices of recalls and market withdrawals from the firms involved as a service to consumers, the media, and other interested parties. FDA does not endorse either the product or the company. This listserv covers mainly Class I (life-threatening) recalls. A complete listing of recalls can be found in the FDA Enforcement Report at: http://www.fda.gov/opacom/Enforce.html



Sierra Pet Products, LLC Issues Nationwide Recall of "Harmony Farms" Canned Dog Foods, "Harmony Farms" Canned Cat Foods and "Harmony Farms" Dog Treats Manufactured at American Nutrition, Inc.

Contact:
Caryn Cox
203-762-2525 EXT. 20

FOR IMMEDIATE RELEASE -- April 27, 2007 -- SIERRA PET PRODUCTS, LLC, Wilton, CT, is initiating a nationwide recall of all canned dog foods, all canned cat food and all dog treats sold under its "Harmony Farms" brand. The Company is taking this voluntary action after learning that the FDA has confirmed the presence of melamine, a substance not approved for use in food, in rice protein concentrate used by the contract manufacturer in the production of some of these products.

It should be noted the "Harmony Farms" canned dog and cat food products were not formulated or labeled to contain rice protein concentrate, and that the manufacturer, American Nutrition, Inc. added the rice protein concentrate to these products without Sierra Pet Products' knowledge or consent. For this reason, Sierra Pet Products is concerned that it can not have any faith in the integrity, or the accuracy of the ingredient labels of any of its products manufactured by American Nutrition. Therefore Sierra Pet Products is withdrawing all products manufactured by American Nutrition, including products that American Nutrition claims do not contain rice protein. The FDA investigation into the inclusion of the rice protein by American Nutrition in the "Harmony Farms" products is ongoing.

Consumers who have any of the "Harmony Farms" can dog foods, can cat foods, or dog treats that are being recalled should stop using the products immediately, and return any unused or partially used products to the retailer where they were purchased, for a full refund.

Sierra Pet Products has not received any reports of pet illness from any of the recalled products, but consumers are advised to speak with their veterinarian about any concerns for their pet's health.

The recall includes the following:

All Cans of "Harmony Farms" dog food
All Cans of "Harmony Farms" cat food
All "Harmony Farms" dog treats
NO HARMONY FARMS DRY DOG OR CAT FOODS SOLD IN BAGS ARE MANUFACTURED AT AMERICAN NUTRITION. NONE OF THESE DRY DOG OR CAT FOODS ARE INVOLVED IN THIS RECALL.

FDA has been apprised of this action, and Sierra Pet Products will continue to cooperate with the FDA in its investigation of this matter.

Sierra Pet Products has not received any complaints of illness or renal failure associated with the use of any of the recalled products.

Sierra Pet Products has notified its distributors and retailer customers of this recall by phone and letter and is arranging for return and credit for all recalled products.

Consumers with questions may contact the company at 1-800-808-1664.

####

FDA's Recalls, Market Withdrawals and Safety Alerts Page: http://www.fda.gov/opacom/7alerts.html

[GinaMarie]

Recall -- State Press Release


This listserv covers mainly Class I (life-threatening) recalls. A complete listing of recalls can be found in the FDA Enforcement Report at: http://www.fda.gov/opacom/Enforce.html



Bronson Advises Consumers To Check Refrigerators For Potentially Tainted Cheeses

Contact:
Dr. John Fruin
(850) 245-5520

FOR IMMEDIATE RELEASE -- Tallahassee, FL -- April 27, 2007 -- Florida Agriculture and Consumer Services Commissioner Charles H. Bronson is urging consumers to check their refrigerators for Ole Mexican Foods' Verole Queso Fresco Authentic Mexican Crumbling Cheese and Ole Fresco Authentic Mexican Crumbling Cheese. The two products may be contaminated with E. coli bacteria.

The potential for this contamination was determined after random testing performed by the Florida Department of Agriculture and Consumer Services revealed the presence of E.coli bacteria in samples of both of the cheeses.

"The discovery of this problem demonstrates the importance of an integrated pro-active food safety program, where products from stores and food processors are not only inspected but tested in our labs, as well," Bronson said.

Department inspectors are working with Florida grocery chains to remove any of the potentially tainted cheese from those stores and are checking warehouses in Florida from which the products were distributed. Bronson said his agency has also notified the U.S. Food Drug Administration, which is responsible for the products in other states.

The affected code for Verole Queso Fresco Authentic Mexican Crumbling Cheese Net Wt. 15 oz. is V7&8 052 47193 SELL BY: 05/31/07; the affected code for Ole Fresco Authentic Mexican Crumbling Cheese Net Wt. 12 oz. is V5&6 051 47193 SELL BY: 05/30/07. Consumers who have purchased these products are urged to return them to the place of purchase.

No illnesses have been reported to date in connection with this problem.

####

FDA's Recalls, Market Withdrawals and Safety Alerts Page: http://www.fda.gov/opacom/7alerts.html

~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~

Recall -- FDA Press Release


This listserv covers mainly Class I (life-threatening) recalls. A complete listing of recalls can be found in the FDA Enforcement Report at: http://www.fda.gov/opacom/Enforce.html



FOR IMMEDIATE RELEASE
P07-78
May 2, 2007
Media Inquiries:
Heidi Rebello, 301-827-6242
Consumer Inquiries:
888-INFO-FDA




FDA Requests Recall of All Shelhigh Medical Devices
The U.S. Food and Drug Administration (FDA) today issued a formal written request to Shelhigh, Inc. to recall all of its medical devices remaining in the marketplace, including hospital inventories, because of sterility concerns.

On April 17, 2007, U.S. Marshals, at FDA's request, seized all medical devices including components at Shelhigh's Union, N.J. facility after finding significant deficiencies in the company's manufacturing processes. During the seizure, Shelhigh was asked to perform a voluntary recall of its products, but the company declined.

FDA recommends that doctors and hospitals consider using alternative products. Physicians and patients concerned about Shelhigh devices can visit www.fda.gov/cdrh/safety/041907-shelhigh.html and www.fda.gov/cdrh/medicaldevicesafety/atp/041907-shelhigh.html for more information, including a list of the company's products.

"Since these are critical devices implanted into seriously-ill patients, ensuring their sterility is absolutely essential to prevent infection," said Daniel Schultz, M.D., director, FDA's Center for Devices and Radiological Health. "FDA will continue to provide up-to-date information to patients and physicians about this ongoing public health matter."

The company's deficiencies, described in a complaint filed with the U.S. District Court of New Jersey, may compromise the safety and effectiveness of the devices. Shelhigh's own records indicate a number of sterility test failures and that its testing and retesting procedures were not properly performed.

Shelhigh devices are used in infants, children and adults. The products include pediatric heart valves, tube-like devices for blood flow (conduits), surgical patches, dural patches to aid in tissue recovery after neurosurgery, annuloplasty rings to help repair heart valves, and arterial grafts.

Adverse reactions or quality problems experienced with the use of these products may be reported to FDA's MedWatch Adverse Event Reporting program either online (www.fda.gov/medwatch/report.htm), fax (800-332-0178), or regular mail (use postage-paid FDA form 3500 available at: www.fda.gov/MedWatch/getforms.htm and mail to MedWatch, FDA, 5600 Fishers Lane, Rockville, MD 20852-9787).

####

Questions and Answers



FDA's Recalls, Market Withdrawals and Safety Alerts Page: http://www.fda.gov/opacom/7alerts.html

[GinaMarie]

Recall -- Firm Press Release


FDA posts press releases and other notices of recalls and market withdrawals from the firms involved as a service to consumers, the media, and other interested parties. FDA does not endorse either the product or the company. This listserv covers mainly Class I (life-threatening) recalls. A complete listing of recalls can be found in the FDA Enforcement Report at: http://www.fda.gov/opacom/Enforce.html



Blue Buffalo Company, Ltd Issues Nationwide Recall of "Blue" Canned Dog Foods, "Blue Spa Select" Canned Cat Foods and "Blue" Dog Treats Manufactured At American Nutrition, Inc.

Contact:
David Petrie
203-762-9751 EXT. 17

FOR IMMEDIATE RELEASE -- April 27, 2007 -- Blue Buffalo Company, Ltd, Wilton, CT, is initiating a nationwide recall of all canned dog foods sold under its "Blue" dog food brand, all canned cat food sold under its "Blue Spa Select" cat food brand, and all dog treats sold under its "Blue" dog food brand. The Company is taking this voluntary action after learning that the FDA has confirmed the presence of melamine, a substance not approved for use in food, in rice protein concentrate used by the contract manufacturer in the production of some of these products.

It should be noted the "Blue" canned dog and cat food products were not formulated or labeled to contain rice protein concentrate, and that the manufacturer, American Nutrition, Inc. added the rice protein concentrate to these products without Blue Buffalo Company's knowledge or consent. For this reason, Blue Buffalo Company is concerned that it can not have any faith in the integrity, or the accuracy of the ingredient labels of any of its products manufactured by American Nutrition. Therefore Blue Buffalo is withdrawing all products manufactured by American Nutrition, including products that American Nutrition claims do not contain rice protein. The FDA investigation into the inclusion of the rice protein by American Nutrition in Blue Buffalo's products is ongoing.

Consumers who have any of the "Blue" can dog foods, "Blue Spa Select" can cat foods, or "Blue" dog treats that are being recalled should stop using the products immediately, and return any unused or partially used products to the retailer where they were purchased, for a full refund.

Blue Buffalo has not received any reports of pet illness from any of the recalled products, but consumers are advised to speak with their veterinarian about any concerns for their pet's health.

The recall includes the following:

All Cans of "Blue" dog food
All Cans of "Blue Spa Select" cat food
All "Blue" dog treats

NO BLUE DRY DOG OR CAT FOODS SOLD IN BAGS ARE MANUFACTURED AT AMERICAN NUTRITION. NONE OF THESE DRY DOG OR CAT FOODS ARE INVOLVED IN THIS RECALL.

FDA has been apprised of this action, AND Blue Buffalo will continue to cooperate with the FDA in its investigation of this matter.

Blue Buffalo has not received any complaints of illness or renal failure associated with the use of any of the recalled products.

Blue Buffalo has notified its distributors and retailer customers of this recall by phone and letter and is arranging for return and credit for all recalled products.

Consumers with questions may contact the company at 1-800-919-2833.

####

FDA's Recalls, Market Withdrawals and Safety Alerts Page: http://www.fda.gov/opacom/7alerts.html

~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~

Recall -- Firm Press Release


FDA posts press releases and other notices of recalls and market withdrawals from the firms involved as a service to consumers, the media, and other interested parties. FDA does not endorse either the product or the company. This listserv covers mainly Class I (life-threatening) recalls. A complete listing of recalls can be found in the FDA Enforcement Report at: http://www.fda.gov/opacom/Enforce.html



SmartPak Canine Voluntarily Recalls LiveSmart Weight Management Formula

Contact:
Paal Gisholt 774 773-1100
Consumers:
800 461-8898

FOR IMMEDIATE RELEASE -- PLYMOUTH, MA (April 25, 2007) - Wilbur-Ellis, a San Francisco-based supplier of pet food ingredients, has asked all pet food producers that used their rice protein concentrate to recall dog food produced using that ingredient due to a risk that it may have been contaminated with melamine. Melamine is an industrial chemical used to make plastics and fertilizers that can lead to illness or fatalities in animals if consumed.

SmartPak Canine used rice protein concentrate supplied by Wilbur-Ellis for a single, recently produced batch of its LiveSmart - Weight Management Formula dog food. SmartPak is voluntarily recalling that batch of the product. Virtually all of the potentially contaminated batch was recovered by SmartPak before going to customers; only 45 pet owners received shipments of the affected product and all of them have been contacted. SmartPak has not received any reports of pets taking ill as a result of feeding LiveSmart Weight Management food.

SmartPak learned of this issue last Friday April 20th, when its contract manufacturer, Chenango Valley Pet Food, Inc., informed them that a recently produced batch of LiveSmart Weight Management Formula was manufactured using rice protein concentrate sourced from Wilbur-Ellis. Immediately that day SmartPak: 1) stopped offering the LiveSmart Weight Management Formula product for sale on its website, 2) cancelled all pending orders from its customers for LiveSmart Weight Management Formula, 3) diverted monthly shipments on UPS trucks that had not yet been delivered, and 4) contacted all 45 affected customers via telephone and email, informed them of the situation, and told them to stop feeding the product.

SmartPak Canine also sent a complimentary replacement shipment of SmartPak portion paks containing another national brand of weight management food to ensure a consistent supply of food for their pet and to minimize the likelihood of a consumer continuing to feed the possibly contaminated food.

This was the first and only batch of LiveSmart food containing rice protein concentrate sourced from Wilbur-Ellis. No other LiveSmart foods contain rice protein concentrate as an ingredient. The following LiveSmart formulas do not contain either of the ingredients affected in the recall (rice protein concentrate or wheat gluten) and remain available for sale in portion-pak SmartPaks:

LiveSmart Adult - Chicken and Brown Rice
LiveSmart Senior - Chicken and Brown Rice
LiveSmart Puppy - Chicken and Brown Rice
LiveSmart Adult - Lamb and Brown Rice
Paal Gisholt, SmartPak's President and CEO, commented, "We started SmartPak Canine because we love dogs and wanted to do everything possible to promote their health and well being. We've made it a key focus of our business to promote the feeding of higher quality dog foods, in controlled portions, as the cornerstone of canine health. As pet owners ourselves, our hearts go out to the many thousands of dog and cat lovers who have been affected by this terrible situation."

Consumers with questions about the pet food they use should visit the FDA Web site at www.fda.gov. For more information regarding Wilbur-Ellis' recall, their press release may be viewed at: http://www.fda.gov/oc/po/firmrecalls/wilburellis04_07.html

####



FDA's Recalls, Market Withdrawals and Safety Alerts Page: http://www.fda.gov/opacom/7alerts.html

[GinaMarie]

Recall -- Firm Press Release


FDA posts press releases and other notices of recalls and market withdrawals from the firms involved as a service to consumers, the media, and other interested parties. FDA does not endorse either the product or the company. This listserv covers mainly Class I (life-threatening) recalls. A complete listing of recalls can be found in the FDA Enforcement Report at: http://www.fda.gov/opacom/Enforce.html



Galliker Dairy Issues a Product Recall on Half-Gallons of Acidophilus Plus Reduced Fat Milk

Contact:
Galliker Dairy
800-447-6455

FOR IMMEDIATE RELEASE -- Johnstown, PA -- May 2, 2007 -- Galliker Dairy Company of Johnstown, Pennsylvania, is recalling half-gallon packages of Galliker's Acidophilus Plus Reduced Milk because they possibly contain under-processed milk. Under-processed milk may be unsafe. It has not been shown to be feasible to perform routine bacteriological tests on the raw milk itself to determine the presence or absence of all pathogens and thereby ensure that it is free of infectious organisms. Only products with the code date of May 13, 2007 are involved.

The product comes in a 64-ounce (One Half-Gallon), plastic package marked with the code date on the front of the package. No illnesses have been reported to date in connection with this problem.

The recall was initiated after a chemical test indicated that possible under-processing occurred. All of Galliker's processing documents indicate that the proper procedures were followed. Only this one product is involved.

Production of this product will continue while this incident is investigated. Products having any other code date are not affected.

Retailers are asked to pull-from-sale all unsold Galliker's Acidophilus Plus Reduced Fat Milk with the code date of May 13, 2007 and return them for full refund. Consumers with any questions may contact the company at 800-477-6455.

This recall is being made with the knowledge of the U.S. Food and Drug Administration and the Pennsylvania Department of Agriculture.

####

FDA's Recalls, Market Withdrawals and Safety Alerts Page: http://www.fda.gov/opacom/7alerts.html

~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~

Recall -- Firm Press Release


FDA posts press releases and other notices of recalls and market withdrawals from the firms involved as a service to consumers, the media, and other interested parties. FDA does not endorse either the product or the company. This listserv covers mainly Class I (life-threatening) recalls. A complete listing of recalls can be found in the FDA Enforcement Report at: http://www.fda.gov/opacom/Enforce.html



Galliker Dairy Issues a Product Recall on Half-Gallons of Healthy Chekd Calcium Enriched Fat Free Milk

Contact:
Galliker Dairy
800-477-6455

FOR IMMEDIATE RELEASE -- Johnstown, PA -- May 3, 2007 -- Galliker Dairy Company of Johnstown, Pennsylvania, is recalling half-gallon packages of Galliker's Healthy Chekd Calcium Enriched Fat Free Milk because they are over-fortified with Vitamin A. High levels of Vitamin A can be harmful to people with a Vitamin A sensitivity. Only products coded May 14, 2007 are affected. The product comes in a 64-ounce (One Half-Gallon), plastic package marked with the code date on the front of the package. No illnesses have been reported to date in connection with this problem.

The recall was initiated after a chemical test indicated that over-fortification occurred. All of Galliker's processing documents indicate that the proper procedures were followed. Currently the company and the Pennsylvania Department of Agriculture are reviewing how vitamins are added to this product. Only this one product is involved. All distribution was contained within the state of Pennsylvania.

Production of this product will continue while this incident is investigated. Products having any other code date are not affected.

Retailers are asked to pull-from-sale all unsold Galliker's Healthy Chekd Calcium Enriched Fat Free Milk with the code date of May 14, 2007 and return them for full refund. Consumers with any questions may contact the company at 800-477-6455.

This recall is being made with the knowledge of the US Food and Drug Administration and the Pennsylvania Department of Agriculture.

The UPC for this product is 070474-001766. Thank you for your cooperation and we apologize for any inconvenience.

####

FDA's Recalls, Market Withdrawals and Safety Alerts Page: http://www.fda.gov/opacom/7alerts.html

[GinaMarie]

Recall -- Firm Press Release


Menu Foods Adds to Recall List

Contact:
Media and Investor Relations
Sarah Tuite
(416) 848-1703
Consumers
1-866-895-2708

FOR IMMEDIATE RELEASE -- May 2, 2007 -- Menu Foods has previously recalled wet cat and dog food produced with adulterated wheat gluten supplied by ChemNutra Inc. Menu Foods is now expanding the recall to include cuts and gravy and select other products which do not include ChemNutra wheat gluten but which were manufactured at any of Menu Foods’ plants during the period that ChemNutra wheat gluten was used at that plant, to the extent they have not already been subject to a recall, due to the possibility of cross-contamination. Menu Foods has received a report from a customer and has received study results, both of which indicate cross-contamination.

As a result, Menu advises the public:

Additional items in the United States and Canada have been added to the recall list as shown below. A further two varieties for Europe have been added to the recall list.
The recall dates of those products previously recalled have been modified to include all dates during the period that ChemNutra wheat gluten was used in the applicable Menu plant. All of these products, including the expanded dates, have previously been withdrawn from the market and should already be off the retailer shelves.
Menu estimates that this additional recall represents less than 5% of the products that have already been recalled or withdrawn.

An updated list of the recalled products, including this addition, is available at the Menu Foods website at http://www.menufoods.com.

Cat Food

Look For a Date that Falls within the below date range on The Bottom of Can or Back of Pouch
Product Description
Size
UPC
Can / Pouch

Americas Choice,
Preferred Pet

Dec/06/09 to Jan/24/10
Sliced Chicken/Heart/Liver 24x3oz
3oz
54807-59117
Can

Best Choice

Nov/08/09 to Mar/07/10
Sliced Chicken 24x3oz
3oz
70038-59960
Can

Nov/08/09 to Mar/07/10
Sliced Beef/Gravy 24x5.5oz
5.5oz
70038-36329
Can

Nov/08/08 to Mar/07/09
Sliced Chicken/Gravy 12x5.5oz
5.5oz
81131-69858
Can

Nov/08/08 to Mar/07/09
Variety Pack (S/T/C) 12x5.5oz
5.5oz
81131-69861
Can

Companion

Dec/06/09 to Jan/24/10
Sliced Turkey/Gravy 24x3oz
3oz
88267-00287
Can

Dec/06/09 to Jan/24/10
Sliced Chicken/Heart/Liver 24x3oz
3oz
88267-00288
Can

Dec/06/09 to Jan/24/10
Sliced Beef/Gravy 24x3oz
3oz
88267-00283
Can

Dec/06/09 to Jan/24/10
Variety Pack (Sliced) 24x3oz
3oz
88267-03352
Can


Compliments


Dec/11/09 to Mar/07/10
Chicken Cuts/Gravy 12x374g
374g
55742-35303
Can

Dec/11/09 to Mar/07/10
Beef Cuts/Gravy 12x374g
374g
55742-35301
Can

Dec/06/09 to Jan/24/10
Sliced Beef Platter 24x85g
85g
55742-35279
Can

Dec/06/09 to Jan/24/10
Flaked Trout Platter 24x85g
85g
55742-35285
Can

Dec/06/09 to Jan/24/10
Flaked Tuna Platter 24x85g
85g
55742-35283
Can

Co-Op Gold


Dec/11/09 to Mar/07/10
Chicken/Gravy 24x156g
156g
57316-01070
Can

Dec/06/09 to Jan/24/10
Beef/Gravy 24x156g
156g
57316-01068
Can

Dec/06/09 to Jan/24/10
Sliced Beef/Gravy 24x85g
85g
57316-01064
Can

Demoulas/Market Basket

Dec/06/09 to Jan/24/10
Flaked Trout 24x3oz
3oz
49705-15361
Can

Dec/06/09 to Jan/24/10
Flaked Tuna 24x3oz
3oz
49705-15356
Can

Drs Foster & Smith

Dec/11/09 to Mar/07/10
Chicken/Potato/Carrot/Gravy 24x5.5oz
5.5oz
25141-25280
Can

Fame

Nov/08/09 to Mar/07/10
Sliced Chicken/Gravy 24x5.5oz
5.5oz
45400-27074
Can

Feline Classic

Dec/06/09 to Jan/24/10
Flaked Tuna/Sauce 24x85g
85g
150808
Can

Feline Cuisine

Dec/06/09 to Jan/24/10
Flaked Tuna/Sauce 24x85g
85g
014820
Can

Dec/06/09 to Jan/24/10
Sliced Chicken/Gravy 24x85g
85g
014790
Can

Dec/06/09 to Jan/24/10
Sliced Beef/Gravy 24x85g
85g
014740
Can

Food Lion

Dec/06/09 to Jan/24/10
Flaked Tuna Dinner 24x3oz
3oz
35826-05986
Can

Giant Companion

Dec/06/09 to Jan/24/10
Flaked Tuna 24x3oz
3oz
88267-00286
Can

Dec/11/09 to Mar/07/10
Sliced Chicken/Gravy 12x13.2oz
13.2oz
88267-00334
Can


Giant Eagle

Dec/06/09 to Jan/24/10
Flaked Tuna 24x3oz
3oz
30034-02323
Can

Hannaford

Dec/11/09 to Mar/07/10
Sliced Chicken/Gravy 24x5.5oz
5.5oz
41268-12463
Can

Dec/06/09 to Jan/24/10
Flaked Trout 24x3oz
3oz
41268-13537
Can


Hill Country Fare


Nov/08/09 to Mar/07/10
Sliced Beef/Gravy 24x5.5oz
5.5oz
41220-63411
Can

Hy Vee

Nov/08/09 to Mar/07/10
Sliced Chicken/Grvy 24x5.5oz
5.5oz
75450-05639
Can

Nov/08/09 to Mar/07/10
Sliced Beef/Gravy 24x5.5oz
5.5oz
75450-05640
Can

La Griffe

Dec/11/09 to Mar/07/10
Sliced Chicken/Gravy 24x156g
156g
59749-39750
Can

Dec/06/09 to Jan/24/10
Sliced Beef/Gravy 24x85g
85g
59749-39670
Can

Laura Lynn

Dec/06/09 to Jan/24/10
Flaked Chicken/Tuna 24x3oz
3oz
86854-03790
Can

Dec/06/09 to Jan/24/10
Flaked Salmon/Whitefish 24x3oz
3oz
86854-03886
Can

Dec/06/09 to Jan/24/10
Flaked Trout Dinner 24x3oz
3oz
86854-03788
Can

Master Choice

Dec/11/09 to Mar/07/10
Sliced Chicken/Gravy 12x374g
374g
69200-45121
Can

Dec/11/09 to Mar/07/10
Sliced Beef/Gravy 12x374g
374g
69200-45122
Can

Dec/06/09 to Jan/24/10
Sliced Beef/Gravy 24x85g
85g
69200-45083
Can


Meijer's Main Choice

Dec/06/09 to Jan/24/10
VP (Sliced B/C/T) 24x3oz.
3oz
19283-41177
Can

Dec/06/09 to Jan/24/10
Sliced Beef/Gravy 24x3oz
3oz
19283-41174
Can

Natural Ultramix

Dec/06/09 to Jan/24/10
Adult Salmon/Vegetable/Gravy 24x3oz
3oz
80872-07953
Can

Dec/06/09 to Jan/24/10
Adult Turkey/Vegetable/Gravy 24x3oz
3oz
80872-07955
Can

Dec/06/09 to Jan/24/10
Indoor Chicken/Vegetable/Gravy 24x3oz
3oz
80872-07961
Can

Dec/06/09 to Jan/24/10
Adult Chicken/Vegetable/Gravy 24x3oz
3oz
80872-07951
Can

Nu Pet

Nov/08/09 to Mar/07/10
Sliced Tuna 24x3oz
3oz
71754-41291
Can

Nov/08/09 to Mar/07/10
Sliced Chicken 24x5.5oz
5.5oz
71754-41121
Can

Nutriplan

Dec/06/09 to Jan/24/10
Flaked Tuna Dinner 24x3oz
3oz
41130-06811
Can

Nutro

Dec/06/09 to Jan/24/10
Kitten Beef/Chicken 24x3oz
3oz
79105-35203
Can

Dec/06/09 to Jan/24/10
Kitten Chicken/Oceanfish 24x3oz
3oz
79105-38101
Can

Dec/06/09 to Jan/24/10
Kitten Tuna/Chicken 24x3oz
3oz
79105-35204
Can

Paws

Dec/06/09 to Jan/24/10
Sliced Chicken/Heart/Liver 24x3oz
3oz
36800-08691
Can

Dec/06/09 to Jan/24/10
Sliced Beef/Gravy 24x3oz
3oz
36800-08248
Can

Dec/06/09 to Jan/24/10
Flaked Tuna 24x3oz
3oz
36800-08251
Can

Performatrin Ultra

Dec/06/09 to Jan/24/10
Chicken Stew Flaked 24x156g
156g
15180
Can

Pet Pride

Dec/06/09 to Jan/24/10
Sliced Chicken/Heart/Liver 24x3oz
3oz
11110-86261
Can

Dec/06/09 to Jan/24/10
Sliced Variety Pack 24x3oz
3oz
11110-86003
Can

Nov/08/09 to Mar/07/10
Shredded Turkey/Cheese 24x5.5oz
5.5oz
11110-84878
Can

Presidents Choice

Dec/06/09 to Jan/24/10
Sliced Beef/Gravy 24x156g
156g
60383-65882
Can

Dec/11/09 to Mar/07/10
Chicken Cuts/Gravy 12x374g
374g
60383-65965
Can

Dec/06/09 to Jan/24/10
Sliced Chicken/Turkey 24x85g
85g
60383-67291
Can

Dec/06/09 to Jan/24/10
Sliced Chicken/Gravy 24x85g
85g
60383-37159
Can

Dec/06/09 to Jan/24/10
Sliced Turkey/Gravy 24x85g
85g
60383-37158
Can



Price Chopper

Dec/06/09 to Jan/24/10
Flaked Tuna Dinner 24x3oz
3oz
41735-12826
Can

Priority Canada

Dec/06/09 to Jan/24/10
Flaked Tuna 24x85g
85g
21130-41398
Can

Priority US

Nov/08/09 to Mar/07/10
Chunky Chicken 24x3oz
3oz
21130-41293
Can

Nov/08/09 to Mar/07/10
Variety Pack (S/T/T) 24x3oz
3oz
21130-41397
Can

Nov/08/09 to Mar/07/10
Sliced Tuna Feast 24x3oz
3oz
21130-41344
Can

Roche Brothers

Dec/06/09 to Jan/24/10
Sliced Beef/Gravy 24x3oz
3oz
39639-09711
Can
Roundy's

Dec/06/09 to Jan/24/10
Flaked Fish/Shrimp 24x3oz
3oz
11150-78478
Can

Continued on next post..

[GinaMarie]

Schnucks

Nov/08/09 to Mar/07/10
Sliced Tuna/Gravy 24x3oz
3oz
41318-07087
Can

Nov/08/09 to Mar/07/10
Sliced Chicken/Gravy 24x5.5oz
5.5oz
41318-07102
Can

Nov/08/09 to Mar/07/10
Sliced Beef/Gravy 24x5.5oz
5.5oz
41318-07099
Can

Sophistacat

Nov/08/09 to Mar/07/10
Beef Cuts/Gravy 12x13.2oz
13.2oz
37257-01328
Can

Nov/08/09 to Mar/07/10
Chicken Cuts/Gravy 12x13.2oz
13.2oz
37257-01327
Can

Nov/08/09 to Mar/07/10
Flaked Tuna/Egg/Sauce 24x5.5oz
5.5oz
37257-41106
Can

Nov/08/09 to Mar/07/10
Flaked Tuna/Sauce 24x5.5oz
5.5oz
37257-41107
Can

Nov/08/09 to Mar/07/10
Sliced Chicken/Gravy 24x5.5oz
5.5oz
37257-01311
Can

Nov/08/09 to Mar/07/10
Sliced Chicken/Salmon/Gravy 24x5.5oz
5.5oz
37257-01316
Can

Nov/08/09 to Mar/07/10
Sliced SD Chicken/Gravy 24x5.5oz
5.5oz
37257-01309
Can

Nov/08/09 to Mar/07/10
Sliced Turkey/Liver/Gravy 24x5.5oz
5.5oz
37257-01313
Can

Nov/08/09 to Mar/07/10
Sliced Whitefish/Gravy 24x5.5oz
5.5oz
37257-01314
Can

Nov/08/09 to Mar/07/10
Sliced Beef/Gravy 24x5.5oz
5.5oz
37257-01312
Can

Nov/08/09 to Mar/07/10
Sliced Tuna/Gravy 24x5.5oz
5.5oz
37257-01315
Can

Special Kitty Canada

Dec/11/09 to Mar/07/10
Sliced Chicken/Grvy 24x156g
156g
78742-64597
Can

Dec/06/09 to Jan/24/10
Sliced Beef/Gravy 24x156g
156g
78742-64598
Can

Springfield Prize

Nov/08/09 to Mar/07/10
Sliced Beef/Gravy 24x5.5oz
5.5oz
41380-13806
Can


Triumph

Nov/08/08 to Mar/07/09
Pouch Turkey/Giblets 24x3oz
3oz
73657-00332
Pouch

Nov/08/08 to Mar/07/09
Pouch Mixed Grill 24x3oz
3oz
73657-00334
Pouch

Dec/06/09 to Jan/24/10
Sliced Beef/Gravy 24x3oz
3oz
73657-00167
Can


Wegmans

Dec/06/09 to Jan/24/10
Sliced Beef/Gravy 24x3oz
3oz
77890-76381
Can

Western Family Canada

Dec/06/09 to Jan/24/10
Flaked Tuna 24x85g
85g
62639-81183
Can

White Rose

Nov/08/09 to Mar/07/10
Shredded Turkey/Cheese 24x5.5oz
5.5oz
74807-34377
Can


Winn Dixie

Dec/06/09 to Jan/24/10
Flaked Tuna 24x3oz
85g
21140-18632
Can

Your Pet

Dec/06/09 to Jan/24/10
Flaked Tuna 24x3oz
3oz
72036-40010
Can

Dec/06/09 to Jan/24/10
Sliced Chicken/Heart/Liver 24x3oz
3oz
72036-29028
Can


Dog Food

Look For a Date on The Bottom of Can or Back of Pouch That Falls Within The Below Date Range
Product Description
Size
UPC
Can / Pouch

Authority


Nov/08/09 to Mar/07/10
Lite Chicken/Rice/Gravy 12x14oz
14oz
37257-12044
Can

Nov/08/09 to Mar/07/10
Adult Lamb/Rice/Cuts 24x6oz
6oz
37257-36971
Can

Award

Nov/08/09 to Mar/07/10
Sliced Beef Casserole 24x5.5oz
5.5oz
37257-00504
Can

Nov/08/09 to Mar/07/10
Sliced Chicken Casserole 24x5.5oz
5.5oz
37257-00502
Can

Nov/08/09 to Mar/07/10
Sliced Chicken/Gravy 24x5.5oz
5.5oz
37257-00432
Can

Nov/08/09 to Mar/07/10
Sliced Beef/Gravy 24x5.5oz
5.5oz
37257-00431
Can

Best Choice

Nov/08/09 to Mar/07/10
Beef Liver Cuts/Gravy 12x13.2oz
13.2oz
70038-60079
Can

Nov/08/09 to Mar/07/10
with Beef/Liver Cuts/Gravy 12x22oz
22oz
70038-60082
Can

Nov/08/09 to Mar/07/10
with Beef Cuts/Gravy 12x22oz
22oz
70038-60081
Can

Nov/08/09 to Mar/07/10
with Chicken Cuts/Gravy 12x22oz
22oz
70038-60085
Can


Compliments

Dec/11/09 to Mar/07/10
With Chicken Cuts/Gravy 12x374g
374g
55742-35390
Can

Dec/11/09 to Mar/07/10
With Beef Cuts/Gravy 12x374g
374g
55742-35307
Can

Dec/06/09 to Jan/24/10
Country Stew Cuts/Gravy 12x624g
624g
55742-35387
Can

Dec/06/09 to Jan/24/10
With Lamb/Veg Cuts/Gravy 12x624g
624g
55742-35315
Can

Dec/06/09 to Jan/24/10
With Beef Cuts/Gravy 12x624g
624g
55742-35311
Can

Dec/06/09 to Jan/24/10
With Chicken Cuts/Gravy 12x624g
624g
55742-35310
Can

Co-Op Gold

Dec/11/09 to Mar/07/10
Stew Cuts/Gravy 12x374g
374g
57316-01079
Can

Dec/11/09 to Mar/07/10
Chicken Cuts/Gravy 12x374g
374g
57316-01077
Can

Dec/11/09 to Mar/07/10
Beef Cuts/Gravy 12x374g
374g
57316-01075
Can

Dec/11/09 to Mar/07/10
Stew Cuts/Gravy 12x624g
624g
57316-01082
Can

Dec/11/09 to Mar/07/10
Chicken Cuts/Gravy 12x624g
624g
57316-01081
Can

Dec/06/09 to Jan/24/10
Beef Cuts/Gravy 12x624g
624g
57316-01080
Can


Hannaford

Dec/11/09 to Mar/07/10
Country Stew Cuts/Gravy 12x22oz
22oz
41268-13533
Can

Dec/11/09 to Mar/07/10
Chicken Cuts/Gravy 12x22oz
22oz
41268-12292
Can

Health Diet Gourmet Cuisine

Dec/06/09 to Jan/24/10
Sliced Beef/Gravy 24x156g
156g
78198-01515
Can

Dec/11/09 to Mar/07/10
Sliced Beef 12x374g
374g
78198-01519
Can

Dec/11/09 to Mar/07/10
Country Stew Cuts/Gravy 12x624g
624g
78198-01529
Can

Dec/11/09 to Mar/07/10
Chicken Cut/Gravy 12x624g
624g
78198-01527
Can

Dec/11/09 to Mar/07/10
Beef Cut/Gravy 12x624g
624g
78198-01524
Can

Hill Country Fare

Nov/08/09 to Mar/07/10
Ctry Stew Cuts/Gravy 12x13.2oz
13.2oz
41220-68712
Can

Nov/08/09 to Mar/07/10
Bbq Beef Cuts/Gravy 12x13.2oz
13.2oz
41220-68711
Can

Nov/08/09 to Mar/07/10
Country Stew/Gravy 12x22oz
22oz
41220-67531
Can

Nov/08/09 to Mar/07/10
Beef Cuts/Gravy 12x22oz
22oz
41220-00864
Can

Nov/08/09 to Mar/07/10
Chicken Cuts/Gravy 12x22oz
22oz
41220-68715
Can

Nov/08/09 to Mar/07/10
Beef Cuts/Gravy 6x22oz
22oz
41220-67532
Can

Nov/08/09 to Mar/07/10
Lamb/Vegetable/Gravy 12x22oz
22oz
41220-67530
Can

Nov/08/09 to Mar/07/10
Sliced Bbq Beef/Gravy 24x5.5oz
5.5oz
41220-05168
Can

Nov/08/09 to Mar/07/10
Sliced Bbq Chicken/Gravy 24x5.5oz
5.5oz
41220-05169
Can

Nov/08/09 to Mar/07/10
Sliced Chicken/Gravy 24x5.5oz
5.5oz
41220-68708
Can

Hy Vee

Nov/08/09 to Mar/07/10
Chicken Cuts/Gravy 12x13.2oz
13.2oz
75450-05606
Can

Nov/08/09 to Mar/07/10
Stew Cuts/Gravy 12x13.2oz
13.2oz
75450-05572
Can

Nov/08/09 to Mar/07/10
Beef/Liver Cuts/Gravy 12x13.2oz
13.2oz
75450-05604
Can

Nov/08/09 to Mar/07/10
Beef Cuts/Gravy 12x22oz
22oz
75450-05608
Can

Nov/08/09 to Mar/07/10
Beef/Liver Cuts/Gravy 12x22oz
22oz
75450-05611
Can

Nov/08/09 to Mar/07/10
Sliced Chicken/Gravy 24x5.5oz
5.5oz
75450-05561
Can

Nov/08/09 to Mar/07/10
Sliced Beef/Gravy 24x5.5oz
5.5oz
75450-05546
Can

La Griffe

Dec/11/09 to Mar/07/10
Chicken Cuts/Gravy 12x624g
624g
59749-39662
Can

Dec/06/09 to Jan/24/10
Beef Cuts/Gravy 12x624g
624g
59749-39654
Can

continued on next post...

[GinaMarie]

Master Choice

Dec/11/09 to Mar/07/10
Chicken Cuts/Gravy 12x374g
374g
69200-45163
Can

Dec/06/09 to Jan/24/10
Country Stew Cuts/Gravy 12x624g
624g
69200-45187
Can

Dec/06/09 to Jan/24/10
Beef Cuts/Gravy 12x624g
624g
69200-45182
Can

Dec/06/09 to Jan/24/10
Chicken Cuts/Gravy 12x624g
624g
69200-45185
Can

Natural Life

Nov/08/09 to Mar/07/10
Lamaderm 12x13.2oz
13.2oz
12344-06114
Can

Nov/08/09 to Mar/07/10
Puppy 12x13.2oz
13.2oz
12344-01114
Can


Nov/08/09 to Mar/07/10
Sliced Chicken/Gravy 12x22oz
22oz
71754-41315
Can

Nov/08/09 to Mar/07/10
Beef Cuts/Gravy 12x22oz
22oz
71754-41249
Can

Nov/08/09 to Mar/07/10
Beef Stew Cuts/Gravy 12x22oz
22oz
71754-41250
Can

Nov/08/09 to Mar/07/10
Lamb/Vegetable Cuts/Gravy 12x22oz
22oz
71754-41292
Can

Nov/08/09 to Mar/07/10
Sliced Chicken/Gravy 24x5.5oz
5.5oz
71754-41315
Can


Ol' Roy Canada

Dec/11/09 to Mar/07/10
Chicken Cuts Value Pack 12x374g
374g
78742-52011
Can

Dec/11/09 to Mar/07/10
Beef Cuts Value Pack 12x374g
374g
78742-52019
Can

Dec/11/09 to Mar/07/10
Country Stew Cuts/Gravy 12x374g
374g
78742-64516
Can

Dec/11/09 to Mar/07/10
Beef Cuts/Gravy 12x374g
374g
78742-51403
Can

Dec/11/09 to Mar/07/10
Chicken Cuts/Gravy 12x374g
374g
78742-51411
Can

Dec/11/09 to Mar/07/10
Beef/Liver Cuts/Gravy 12x374g
374g
78742-64515
Can

Dec/06/09 to Jan/24/10
With Beef/Bacon/Cheese Cuts 12x624g
624g
78742-51433
Can

Dec/06/09 to Jan/24/10
With Beef/Barley Cuts 12x624g
624g
78742-51425
Can

Dec/06/09 to Jan/24/10
Country Stew Cuts/Gravy 12x624g
624g
78742-64520
Can

Dec/06/09 to Jan/24/10
Beef Cuts/Gravy 12x624g
624g
78742-51435
Can

Dec/11/09 to Mar/07/10
Chicken Cuts/Gravy 12x624g
624g
78742-51388
Can

Dec/11/09 to Mar/07/10
With Lamb/Vegetable Cuts 12x624g
624g
78742-52132
Can

Dec/06/09 to Jan/24/10
Beef/Liver Cuts/Gravy 12x624g
624g
78742-64519
Can

Performatrin Ultra

Dec/06/09 to Jan/24/10
Chicken/Rice Stew 12x374g
374g
78198-01776
Can

Dec/06/09 to Jan/24/10
Lamb/Rice Stew 12x374g
374g
78198-01775
Can


Pet Pride / Good n Meaty

Nov/08/09 to Mar/07/10
Beef/Liver Cuts/Gravy 12x22oz
22oz
11110-86232
Can

Nov/08/09 to Mar/07/10
Sliced Beef/Gravy 24x5.5oz
5.5oz
11110-86025
Can

Presidents Choice

Dec/11/09 to Mar/07/10
Sliced Chicken/Gravy 24x156g
156g
60383-64167
Can

Dec/06/09 to Mar/07/10
Sliced Beef/Gravy 24x156g
156g
60383-64168
Can

Dec/11/09 to Mar/07/10
Beef Cuts/Gravy 12x374g
374g
60383-37457
Can

Dec/11/09 to Mar/07/10
Chicken Cuts/Gravy 12x374g
374g
60383-37459
Can

Dec/06/09 to Jan/24/10
Chicken & Veal Cuts/Gravy 12x624g
624g
60383-68762
Can

Dec/11/09 to Mar/07/10
Beef Cuts/Gravy 12x624g
624g
60383-37456
Can

Dec/11/09 to Mar/07/10
Beef Stew Cuts/Gravy 12x624g
624g
60383-65895
Can

Dec/11/09 to Mar/07/10
Chicken Cuts/Gravy 12x624g
624g
60383-37458
Can

Dec/11/09 to Mar/07/10
Extra Meaty Beef/Bacon/Cheese 12x624g
624g
60383-67619
Can

Dec/11/09 to Mar/07/10
Extra Meaty Beef/Chicken Cuts 12x624g
624g
60383-67618
Can

Dec/11/09 to Mar/07/10
Extra Meaty Beef/Barley/Cuts 12x624g
624g
60383-67620
Can

Priority US

Nov/08/09 to Mar/07/10
Beef Cuts/Gravy 6x22oz
22oz
21130-42017
Can

Nov/08/09 to Mar/07/10
Sliced Chicken/Gravy 24x5.5oz
5.5oz
21130-42007
Can

Schnucks

Nov/08/09 to Mar/07/10
Chicken Cuts/Gravy 12x13.2oz
13.2oz
41318-07121
Can

Nov/08/09 to Mar/07/10
Stew Cuts/Gravy 12x13.2oz
13.2oz
41318-07123
Can

Nov/08/09 to Mar/07/10
Beef/Liver Cuts/Gravy 12x13.2oz
13.2oz
41318-07118
Can

Nov/08/09 to Mar/07/10
Sliced Turkey/Gravy 24x5.5oz
5.5oz
41318-07108
Can

Nov/08/09 to Mar/07/10
With Beef Cuts/Gravy 12x22oz
22oz
41318-07146
Can

Nov/08/09 to Mar/07/10
With Chopped Beef 12x22oz
22oz
41318-07147
Can

Springfield Prize

Nov/08/09 to Mar/07/10
Country Stew Cuts/Gravy 12x13.2o
13.2oz
41380-13908
Can

Nov/08/09 to Mar/07/10
Country Stew Cuts/Gravy 12x22oz
22oz
41380-13907
Can

Nov/08/09 to Mar/07/10
Lamb/Vegetable/Cuts/Gravy 12x22oz
22oz
41380-13891
Can

Nov/08/09 to Mar/07/10
Chicken Cuts/Gravy 12x22oz
22oz
41380-13904
Can

Nov/08/09 to Mar/07/10
Beef Cuts/Gravy 12x22oz
22oz
41380-13890
Can

Nov/08/09 to Mar/07/10
Sliced Chicken/Gravy 24x5.5oz
5.5oz
41380-14291
Can


Stater Brothers

Nov/08/09 to Mar/07/10
with Beef/Liver Cuts in Gravy 12x22
22oz
74175-12359
Can

Nov/08/09 to Mar/07/10
with Chicken Cuts/Gravy 12x22oz
22oz
74175-12280
Can

Nov/08/09 to Mar/07/10
with Lamb/Vegetable Cuts/Gravy 12x22o
22oz
74175-12357
Can

Nov/08/09 to Mar/07/10
Country Stew Cuts/Gravy 12x22oz
22oz
74175-12283
Can

Nov/08/09 to Mar/07/10
with Beef Cuts/Gravy 12x22oz
22oz
74175-12282
Can

Nov/08/09 to Mar/07/10
Sliced Beef/Gravy 24x5.5oz
5.5oz
74175-12351
Can

Triumph

Dec/11/09 to Mar/07/10
Sliced Beef/Gravy 24x5.5oz
5.5oz
73657-00171
Can

Truly

Dec/11/09 to Mar/07/10
Beef/Liver Cuts/Gravy 12x624g
624g
00364-41665
Can

Dec/11/09 to Mar/07/10
Country Stew Cuts/Gravy 12x624g
624g
00364-41806
Can

Dec/11/09 to Mar/07/10
Chicken Cuts/Gravy 12x624g
624g
00364-49564
Can

Dec/11/09 to Mar/07/10
Beef Cuts/Gravy 12x624g
624g
00364-42036
Can

Western Family Canada

Dec/11/09 to Mar/07/10
Country Stew Cuts/Gravy 12x374g
374g
62639-19579
Can

Dec/11/09 to Mar/07/10
Chicken Cuts/Gravy 12x374g
374g
62639-19580
Can

Dec/11/09 to Mar/07/10
Lamb/Vegetable Cuts 12x624g
624g
62639-29264
Can

Dec/06/09 to Jan/24/10
Beef Cuts/Gravy 12x624g
624g
62639-19587
Can

Dec/06/09 to Jan/24/10
Beef/Liver Cuts/Gravy 12x624g
624g
62639-19588
Can

Dec/06/09 to Jan/24/10
Stew Cuts/Gravy 12x624g
624g
62639-19590
Can

Western Family US

Nov/08/09 to Mar/07/10
Beef/Liver/Cuts 12x13.2oz
13.2oz
15400-04070
Can

Nov/08/09 to Mar/07/10
Stew Cuts 12x13.2oz
13.2oz
15400-04069
Can

Nov/08/09 to Mar/07/10
Sliced Beef/Gravy 24x5.5oz
5.5oz
15400-05192
Can

####

FDA's Recalls, Market Withdrawals and Safety Alerts Page: http://www.fda.gov/opacom/7alerts.html

[GinaMarie]

Recall -- Firm Press Release


FDA posts press releases and other notices of recalls and market withdrawals from the firms involved as a service to consumers, the media, and other interested parties. FDA does not endorse either the product or the company. This listserv covers mainly Class I (life-threatening) recalls. A complete listing of recalls can be found in the FDA Enforcement Report at: http://www.fda.gov/opacom/Enforce.html



Aulcorp Food Marketers Inc. Conducts Nationwide Recall of Archer Farms Four Cheese Risotto, 6 oz., "Best if Used by 16JUL2008AA" Because of Possible Health Risk

Contact:
Target Guest Relations
1-800-440-0680

FOR IMMEDIATE RELEASE -- May 4, 2007 -- AULCORP FOOD MARKETERS INC. of TORONTO, ONTARIO, CANADA is recalling Archer Farms FOUR CHEESE RISOTTO flavor, 6 oz., with "Best If Used By 16JUL2008AA", because it has the potential to be contaminated with Salmonella. Salmonella is an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Healthy persons infected with Salmonella often experience fever, diarrhea (which may be bloody), nausea, vomiting and abdominal pain. In rare circumstances, infection with Salmonella can result in the organism getting into the bloodstream and producing more severe illnesses such as arterial infections (i.e., infected aneurysms), endocarditis and arthritis.

No illnesses have been reported to date.

ARCHER FARMS FOUR CHEESE RISOTTO, Code "Best If Used By 16JUL2008AA" was sold nationwide through Target stores. The Archer Farms Four Cheese Risotto flavor has been pulled from Target stores while the FDA and Aulcorp Food Marketers Inc. continue their investigation as to the source of the contamination.

The ARCHER FARMS FOUR CHEESE RISOTTO is packaged in a 6 oz. (170g) Paperboard Box with a mustard yellow banner which identifies this item as the Four Cheese flavor.

The Salmonella contamination was noted after random testing by the US Food and Drug Administration.

Consumers who have purchased the 6 oz.(170 g) packages of ARCHER FARMS FOUR CHEESE RISOTTO, Code "Best If Used By 16JUL2008AA", are urged to return the item to the nearest Target store for a full refund. Consumers with questions may contact Target Guest Relations at 1-800-440-0680.

####



FDA's Recalls, Market Withdrawals and Safety Alerts Page: http://www.fda.gov/opacom/7alerts.html

~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~

Recall -- Firm Press Release


FDA posts press releases and other notices of recalls and market withdrawals from the firms involved as a service to consumers, the media, and other interested parties. FDA does not endorse either the product or the company. This listserv covers mainly Class I (life-threatening) recalls. A complete listing of recalls can be found in the FDA Enforcement Report at: http://www.fda.gov/opacom/Enforce.html



Ortho-Clinical Diagnostics, Inc. Issues Voluntary, Nationwide Recall for Cardiac Marker
Contact:
Steve Dnistrian
(908) 218-8287

FOR IMMEDIATE RELEASE -- RARITAN, N.J., May 4 – Ortho-Clinical Diagnostics, Inc. has initiated a voluntary, nationwide recall of two lots of a diagnostic test used by physicians to aid in the diagnosis of injury to heart muscle and/or heart attack because of shifts in test results that could contribute to a missed diagnosis of myocardial infarction.

The company initiated the voluntary recall of the VITROS® Immunodiagnostic Products Troponin I Reagent Pack, Lots 3151 and 3170, after a small number of clinical laboratories administering the test reported shifts in quality control results. An investigation by Ortho-Clinical Diagnostics determined that the potential existed for false negative troponin-I results at very low levels of troponin elevation. A false negative test result would indicate that a person has not had a heart attack or heart muscle injury when in fact they have. Ortho-Clinical Diagnostics is working to identify the root cause of the reported issue.

The recall is limited to the VITROS® Immunodiagnostic Products Troponin I Reagent Pack, Lots 3151 and 3170. Clinical labs in possession of these lots have been contacted via phone, fax and overnight mail by the company and instructed to (a) discontinue use of this product and (b) notify healthcare providers who ordered the test in recent weeks. The identified product lots were distributed to clinical labs in the United States and outside the U.S. between January and March of 2007. Replacement product has been provided to clinical labs with the affected product lots.

Ortho Clinical-Diagnostics has reported the action to the U.S. Food and Drug Administration. No injuries have been reported to date.

A troponin I test is usually ordered, along with other cardiac tests, in the hospital to determine if a patient has had a heart attack or injury to heart muscle. The test, conducted using a sample of the patient’s blood, aids in the diagnosis of myocardial injury or infarction. The results of troponin I tests should be used in conjunction with other diagnostic information including other cardiac markers, ECG, clinical observations and symptoms.

Clinical laboratories with questions may contact the company at 1-800-421-3311.

Any adverse reactions experienced with the use of this product, and/or quality problems should also be reported to the FDA’s MedWatch Program by phone at 1-800-FDA-1088, by Fax at 1-800-FDA-0178, by mail at MedWatch, HF-2, FDA, 5600 Fishers Lane, Rockville, MD 20852-9787, or on the MedWatch website at www.fda.gov/medwatch.

####



FDA's Recalls, Market Withdrawals and Safety Alerts Page: http://www.fda.gov/opacom/7alerts.html

[GinaMarie]

FDA/USDA Joint News Release: Scientists Conclude Very Low Risk to Humans

from Food Containing Melamine



Media Inquiries:
FDA Press Office: 301-827-6242
USDA Press Office: 202-720-4623

Consumer Inquiries:
888-INFO-FDA



May 7, 2007



There is very low risk to human health from consuming meat from hogs and chickens known to have been fed animal feed supplemented with pet food scraps that contained melamine and melamine-related compounds, according to an assessment conducted by scientists from five federal agencies.

In the most extreme risk assessment scenario, when scientists assumed that all the solid food a person consumes in an entire day was contaminated with melamine at the levels observed in animals fed contaminated feed, the potential exposure was about 2,500 times lower than the dose considered safe. In other words, it was well below any level of public health concern.

The risk assessment is an important new science-based component of the continuing federal joint investigation into imported wheat gluten and rice protein concentrate from China that contained melamine and melamine-related compounds.

The risk assessment was conducted by scientists from the Food and Drug Administration (FDA) and the Centers for Disease Control and Prevention (CDC) of the Department of Health and Human Services (HHS), the Environmental Protection Agency (EPA), U.S. Customs and Border Protection (CBP) of the Department of Homeland Security (DHS) and the Food Safety and Inspection Service (FSIS) of the U.S. Department of Agriculture (USDA). This team is now compiling a scientific assessment of the risk to animal health associated with ingestion of animal feed containing melamine and its compounds.

FDA and USDA are in the process of identifying a group of experts to convene a scientific advisory board that would be charged with reviewing the risk assessment. This group would also be asked to contribute to future scientific analysis related to the risk of melamine and its compounds to humans and animals.

In the course of the investigation, it was discovered that pet food was contaminated by wheat gluten and rice protein concentrate that contained melamine and its compounds. Subsequently, scraps of contaminated pet food that contained only low levels of melamine were distributed to farms in a limited number of states and added to the feed consumed by swine and poultry. These scraps constituted only a small percentage of the farm animal rations. In addition, melamine is known to be excreted in animal urine. When exposure levels are much higher, as was the case with cats and dogs, the melamine and its compounds appear to cause the formation of crystals in the kidney systems, resulting in kidney damage. There was no indication of kidney damage in hogs. Both hogs and chickens known to have been fed contaminated feed appear to be healthy.

This dilution factor was an important piece of data considered in the multi-agency science-based human risk analysis and helps to support the conclusion that there is very low risk to human health from eating meat from animals that were fed the contaminated product. This conclusion supports the decision announced on April 28 not to recall meat from animals that were fed contaminated product.

Currently, swine and poultry on farms suspected of receiving contaminated feed are being held under state quarantine or voluntarily by the owners. In several cases, feed samples have tested negative for melamine and related compounds. These tests were conducted by federal laboratories or state laboratories using approved methods. It is assumed that because only small amounts of the contaminated feed were mixed with other rations, the melamine and related compounds were no longer detectable. USDA has concluded that, based on the human risk assessment and the inability to detect melamine in the feed samples, these animals no longer need to be quarantined or withheld from processing.

In other cases, feed samples have tested positive for melamine and related compounds; feed samples were not available; or feed samples have not yet been submitted for testing. These animals continue to be withheld from processing, but are not yet being culled, pending the results of the animal risk assessment. This assessment is expected to be completed within one week. At that time, USDA will determine whether these animals can be released for inspection and further processing.

USDA and FDA continue to conduct a full and comprehensive investigation. As additional information is confirmed, updates will be provided and decisions will be made using the best available science to protect the public's health.

To ensure no further contaminated products enter the U.S., the federal government will continue to monitor imported wheat and corn gluten as well as rice protein concentrate and isolates arriving from all countries destined for human and animal consumption. The FDA import alert for these products sourced from China remains in effect and U.S. Customs and Border Protection will continue laboratory testing of the products as they enter the U.S. The inspections are a precautionary measure to ensure the safety of products entering at U.S. ports of entry. There is no evidence to suggest products bound for the human food supply are contaminated.

For additional information about the pet food and contaminated feed investigation, go to www.fda.gov or www.usda.gov. The human safety/risk assessment will be available online upon completion of an executive summary.

####

USDA Fact Sheet : Melamine and Analogues Safety/Risk Assessment

[GinaMarie]

FDA News Release


FOR IMMEDIATE RELEASE
P07-86
May 10, 2007 Media Inquiries:
301-827-6242
Consumer Inquiries:
888-INFO-FDA


FDA Issues Health Risk Alert for 'True Man' and 'Energy Max' Products

The Food and Drug Administration (FDA) is advising consumers not to purchase or use "True Man" or "Energy Max" products promoted and sold as dietary supplements throughout the United States. Both products -- touted as sexual enhancement products and as treatments for erectile dysfunction (ED) -- are illegal drug products that contain potentially harmful, undeclared ingredients.The products contain substances called analogs that have similar structures to active ingredients in approved prescription drugs.

Consumers should discontinue use of True Man and Energy Max and consult their health care professional about approved treatments for ED.FDA encourages men who experience ED to seek guidance from a health care professional.

FDA has not approved True Man and Energy Max; therefore the safety and effectiveness of these products are unknown. Both products are often advertised as "all natural" alternatives to approved ED drugs in advertisements appearing in newspapers, retail stores, and on the Internet.

"These products threaten the health of the people using them because they contain undeclared chemicals that are similar to the active ingredients used in FDA-approved prescription drug products," said Steven Galson, M.D., MPH, director of the FDA's Center for Drug Evaluation and Research."The risk is even more serious because consumers may not know that these ingredients can interact with medications and dangerously lower their blood pressure."

The undeclared analog ingredients in True Man and Energy Max may interact with nitrates found in some prescription drugs such as nitroglycerin and may lower blood pressure to dangerous levels. Men with diabetes, high blood pressure, high cholesterol or heart disease often take nitrates.

FDA chemical analysis revealed that Energy Max contains thione analog of sildenafil, a substance with a structure similar to sildenafil, the active ingredient in Viagra, an FDA-approved drug for ED.Substances like this are called analogs because they have a structure similar to another drug and may cause similar side effects and drug interactions.

True Man contains a thione analog of sildenafil or piperadino vardenafil, an analog of vardenafil, the active ingredient in Levitra, another FDA-approved prescription drug for ED. Neither the thione analog of sildenafil nor piperadino vardenafil are components of approved drug products.

True Man is sold in boxes containing a 10-capsule blister pack. Energy Max is sold in boxes containing two 10-capsule blister packs.Both products are distributed and packed by America True Man Health, Inc., West Covina, Calif.A review of the ingredient statements for both products revealed that neither piperadino vardenafil nor thione analog of sildenafil are listed as an ingredient, even though one or more of those ingredients is present in the products.

Consumers should report adverse events related to these products to MedWatch, the FDA's voluntary reporting program:
www.fda.gov/medwatch/report.htm
(800) 332-1080
Fax: (800) 332-0178
Mail: MedWatch, Food and Drug Administration, 5600 Fishers Lane, Rockville, MD, 20857-9787

For more information, visit: www.fda.gov/bbs/topics/NEWS/2006/NEW01409.html
www.fda.gov/foi/warning_letters/g5911d.htm

####

FDA's Recalls, Market Withdrawals and Safety Alerts Page: http://www.fda.gov/opacom/7alerts.html

[GinaMarie]

Recall -- Firm Press Release


FDA posts press releases and other notices of recalls and market withdrawals from the firms involved as a service to consumers, the media, and other interested parties. FDA does not endorse either the product or the company. This listserv covers mainly Class I (life-threatening) recalls. A complete listing of recalls can be found in the FDA Enforcement Report at: http://www.fda.gov/opacom/Enforce.html



Spectrum Laboratory Products, Inc. Issues Nationwide Recall of Caffeine Citrated, Powder, Purified
Contact:
Martin LaBenz
(310) 516-8000, Ext. 580
Tom Tyner
(310) 516-8000, Ext. 573

FOR IMMEDIATE RELEASE -- Gardena, CA -- May 18, 2007 --. Spectrum Laboratory Products, Inc, (Spectrum), Gardena, California, is initiating a voluntary nationwide recall of Caffeine Citrated, Powder, Purified, after receiving a complaint about potential sub potency. Caffeine Citrated is a cerebral and respiratory stimulant used primarily to treat idiopathic apnea of prematurity. Blood levels of caffeine in patients were determined to be significantly lower than would be expected. The use of sub-potent compounded preparations made may lead to sub-therapeutic caffeine blood levels and an unacceptable risk of respiratory depression. FDA has been apprised of this action.

Caffeine Citrated, Powder, Purified, is identified as Catalog Number CA110. Recalled lots include the following: TS0225, UK0821 and VI1203.

Pharmacies that have used the above lots of Caffeine Citrated, Powder, Purified, should stop using it and contact Spectrum to make arrangements to return it. Caffeine Citrated, Powder, Purified, was distributed to pharmacies, hospitals, two universities, laboratories, and pharmacy distributors. It can be identified by catalog number CA110 and the name “Caffeine Citrated, Powder, Purified” on the label.

No illnesses or injuries related to this product have been reported to date.

Spectrum is notifying its distributors and customers by telephone and recall letter and is arranging for return of all recalled products.

Consumers with questions may contact Stephen Newton at 1-800-791-3210, Ext. 349

Pharmacies are urged to examine their supplies for any of the recalled Caffeine Citrated, Powder, Purified, and immediately discontinue its use. Patients and consumers who suspect that they have received medications in any dosage form made from the three lot numbers of Caffeine Citrated, Powder, Purified, that are being recalled, should contact their pharmacy or physician. Users should also notify FDA of any complaints or problems associated with these products. Any adverse reactions experienced with the use of this product should also be reported to the FDA's MedWatch Program by phone at 1-800-FDA-1088, by Fax at 1-800-FDA-0178, by mail at MedWatch, HF-410, FDA, 5600 Fishers Lane, Rockville, MD 20852-9787, or on the MedWatch website at www.fda.gov/medwatch

####

FDA's Recalls, Market Withdrawals and Safety Alerts Page: http://www.fda.gov/opacom/7alerts.html

[GinaMarie]

Recall -- Firm Press Release


FDA posts press releases and other notices of recalls and market withdrawals from the firms involved as a service to consumers, the media, and other interested parties. FDA does not endorse either the product or the company. This listserv covers mainly Class I (life-threatening) recalls. A complete listing of recalls can be found in the FDA Enforcement Report at: http://www.fda.gov/opacom/Enforce.html



Chenango Valley Pet Foods Expands Voluntary Nationwide Recall of Certain Pet Foods
Contact:
Dennis J. Bobita
(610) 821-0608

FOR IMMEDIATE RELEASE -- May 17, 2007 -- Chenango Valley Pet Foods previously recalled dry pet foods manufactured with a shipment of rice protein concentrate supplied by Wilbur-Ellis that possibly contained melamine contamination. Chenango Valley Pet Foods is now expanding the recall action to include those pet foods that do not contain rice protein concentrate but were manufactured during periods when rice protein concentrate formulas were processed. The recall of these products is precautionary due to the possibility of cross-contamination.

The following dry pet foods are involved in this recall action:

*DOCTORS FOSTER & SMITH LAMB & BROWN RICE FORMULA ADULT DOG FOOD, NET WT. 6 LBS. (UPC 25141 28244), 15 LBS. (25141 30074), and 30 LBS. (UPC 25141 06043); Date Codes: Best By Feb 09 09 and Best By Feb 26 09;

*SHOP RITE REDI-MIXT DOG FOOD FOR DOGS, NET WT. 25 LB. (UPC 41190 00555), Date Code: Code C7107;

*LICK YOUR CHOPS KITTEN & CAT FOOD, NET WEIGHT 4 LBS. (UPC 32976 25915), and 18 LBS. (UPC 32976 25925); Date Code: Best Used By April 29 08;

*SHEP chunk style dog food, NET WT. 20 LBS. (UPC 41498 14142); Date Code: Best By March 14 08;

*8 in 1 Ferret ULTRA-BLEND ADVANCED NUTRITION DIET, NET WT. 20 LBS, UPC 26851 00413, Code: C7072;

*Bulk Lamb & Brown Rice Formula Dog Food, Date Code: Feb 09, 08, sold to one consignee SmartPak.

*Health Diet Cat Food Chicken & Rice Dinner NET WT. 1.81 kg/4 LB (UPC 78198 01594), 4 kg/8.8 LB (UPC 78198 01599), and 8 kg/17.6 LB (UPC 78198 01585); Code C7072;

*EVOLVE KITTEN FORMULA, NET WT. 3 LBS. (UPC 73657 00250) and 7 LBS. (UPC 73657 00251); Date Code: Best Used By Sept 13 08. Evolve has recovered 99.5% of the product from its distributors and is working with dealers to recover the remaining inventory.

No illnesses or injuries related to these products have been reported to date.

Pet owners who have purchased the pet foods listed above should immediately discontinue using the products and return them to the place of purchase for full refund. Pet owners should consult with a veterinarian if they have any health concerns with their pet. Consumers with questions may contact the company at 1-610-821-0608.

####

FDA's Recalls, Market Withdrawals and Safety Alerts Page: http://www.fda.gov/opacom/7alerts.html

[GinaMarie]

Recall -- Firm Press Release


FDA posts press releases and other notices of recalls and market withdrawals from the firms involved as a service to consumers, the media, and other interested parties. FDA does not endorse either the product or the company. This listserv covers mainly Class I (life-threatening) recalls. A complete listing of recalls can be found in the FDA Enforcement Report at: http://www.fda.gov/opacom/Enforce.html



Nutra Nuggets 40 Lb. Lamb Meal and Rice Formula Recalled Due to Cross Contamination
Contact:
Customer Information Center
1-866-214-6945

FOR IMMEDIATE RELEASE -- Meta, MO -- May 23, 2007 -- Diamond Pet Foods announced that it has recalled a limited quantity of Nutra Nuggets 40 Lb. Lamb Meal and Rice Formula because of confirmatory testing that indicates the product may include traces of melamine resulting from cross contamination during manufacturing. No animal deaths have been reported.

This action is limited to Nutra Nuggets 40 Lb. Lamb Meal and Rice Formula with production codes of NLR0404A2SL, "Best Before" Oct. 9, 2008, and NLR0404B2SL, "Best Before" Oct. 9, 2008. The recalled product was manufactured at the company's Lathrop, Calif. facility. No other Nutra Nuggets products are affected.

Consumers who purchased Nutra Nuggets 40 Lb. Lamb Meal and Rice Formula with production codes of NLR0404A2SL, "Best Before" Oct. 9, 2008, and NLR0404B2SL, "Best Before" Oct. 9, 2008, should stop feeding the product immediately and return unused portions to their retailer for a full refund. Consumers may also contact the Diamond Pet Foods Customer Information Center toll free at 1-866-214-6945 for further information. The Center, which is staffed by veterinarians, is open Monday through Friday from 8:00 a.m. to 7:00 p.m. CDT.

####

FDA's Recalls, Market Withdrawals and Safety Alerts Page: http://www.fda.gov/opacom/7alerts.html

[GinaMarie]

Recall -- Firm Press Release


FDA posts press releases and other notices of recalls and market withdrawals from the firms involved as a service to consumers, the media, and other interested parties. FDA does not endorse either the product or the company. This listserv covers mainly Class I (life-threatening) recalls. A complete listing of recalls can be found in the FDA Enforcement Report at: http://www.fda.gov/opacom/Enforce.html



Hong Chang Corporation Recalls Monkfish Because of Possible Health Risk

Contact:
Steven Luo
(562) 309-0068

FOR IMMEDIATE RELEASE -- Santa Fe Springs, CA -- May 23, 2007 -- Hong Chang Corporation, Santa Fe Springs, CA is recalling product labeled as monkfish because it may contain tetrodotoxin, a potent toxin. Although the product was identified as monkfish, we are concerned the product may be pufferfish because this toxin is usually associated with certain types of pufferfish. Consumption of foods containing tetrodotoxin can result in life-threatening illness or death. This toxin cannot be destroyed by cooking or freezing.

Initial symptoms occur within 30 minutes to several hours after consuming food containing the toxin and are characterized by lip and tongue tingling and then followed by facial and extremity tingling and numbness. Subsequent symptoms may include headache, balance problems, excessive salivation, nausea, vomiting, and diarrhea with abdominal pain which can be severe. In severe cases, muscles can become paralyzed and death may follow resulting from respiratory muscle paralysis. Consumers experiencing these symptoms should seek immediate medical care.

A total of 282, 22-lb. boxes of monkfish were distributed to *********rs in Illinois, California and Hawaii beginning in September 2006. This product was sold in retail stores, restaurants, and cash and carry stores in these regions.

The monkfish are individually packaged in clear plastic sleeves and placed in a plastic liner which is inside a cardboard box. There are no lot numbers on the box. The boxes are packed by total weight, 22 pounds, with labeling on one panel that reads "MONK FISH GUTTED AND HEAD-OFF PRODUCT OF CHINA". A second box panel bears nutritional facts and the following, "Ingredients: Monk fish; Imported by: Hong Chang Corp, Santa Fe Springs, CA 90670; Product of China (P.R.C.)."

The problem was discovered after two people in the Chicago, IL area fell ill after consuming soup made with the "monkfish". The Food and Drug Administration's (FDA) analysis of the fish confirmed the presence of life-threatening levels of tetrodotoxin.

At this time, Hong Chang Corp. and FDA are investigating how the problem occurred.

Consumers who have purchased this monkfish are urged to return it to the place of purchase for a full refund. Care should be exercised in handling the fish as the tetrodotoxin may be present on the skin and flesh of the fish. Wash hands thoroughly after handling. Consumers with questions may contact the company at 1-562-309-0068.

Consumers who may have consumed these products and have concerns are encouraged to contact their health care provider. Consumers should also report illnesses associated with consumption of these products to the nearest FDA district offices and to their local health authority.

####



FDA's Recalls, Market Withdrawals and Safety Alerts Page: http://www.fda.gov/opacom/7alerts.html

[GinaMarie]

FDA Press Release


This listserv covers mainly Class I (life-threatening) recalls. A complete listing of recalls can be found in the FDA Enforcement Report at: http://www.fda.gov/opacom/Enforce.html



FOR IMMEDIATE RELEASE
P07-91
May 24, 2007
Media Inquiries:
301-827-6242
Consumer Inquiries:
888-INFO-FDA


FDA Warning on Mislabeled Monkfish
Fish Believed to be Puffer Fish; Contains Deadly Toxin

The Food and Drug Administration (FDA) is warning consumers not to buy or eat imported fish labeled as monkfish, which actually may be puffer fish, containing a potentially deadly toxin called tetrodotoxin. Eating puffer fish that contain this potent toxin can result in serious illness or death.

Tetrodotoxin is not destroyed by common food preparation or storage, such as cooking or freezing. Monkfish do not contain tetrodotoxin.

The product was imported and distributed by Hong Chang Corp., Santa Fe Springs, Calif.

Consumers concerned that they may have purchased this fish should contact their retailer and ask if the product was received from Hong Chang Corp.

The product should not be eaten, it should be thrown away. Care should be exercised in handling the fish, as the tetrodotoxin may be present on the skin and flesh of the fish. Consumers should wash hands thoroughly after handling the fish.

Two people in the Chicago area became ill after consuming homemade soup containing the fish. One was hospitalized due to severe illness.

FDA's analysis of the fish confirmed the presence of potentially life-threatening levels of tetrodotoxin.

Initial symptoms of tetrodotoxin poisoning occur 30 minutes to several hours after food containing the toxin is consumed. Tetrotoxin poisoning is characterized initially by tingling of the lips and tongue. Tingling of the face and extremities and numbness follow. Subsequent symptoms may include headache, balance problems, excessive salivation, nausea, vomiting, diarrhea and abdominal pain. Consumers experiencing these symptoms should seek immediate medical care and are encouraged to report their illness to local health authorities. In severe cases, muscles can become paralyzed, and death may follow from respiratory muscle paralysis.

A total of 282 22-pound boxes labeled as monkfish were distributed to *********rs in Illinois, California and Hawaii beginning in September 2006. These fish were then sold to restaurants or sold in stores. In one instance, the retailer labeled the fish as "bok," the Korean name for puffer fish.

The white 22-pound boxes were labeled in black ink. One box panel is labeled as: "FROZEN MONKFISH GUTTED AND HEAD-OFF" and "PRODUCT OF CHINA." A second panel bears nutritional facts and the following: "Ingredients: Monk fish; Imported by: Hong Chang Corp, Santa Fe Springs, CA 90670; Product of China (P.R.C.)." A third panel has a checkbox indicating the size as either "0.5-1" or "1-2" and shows the net weight as 22 pounds. There are no manufacturing codes on the box. The fish in the box are individually wrapped in plastic bags with no labeling.

FDA allows puffer fish to be imported into the United States only under strict provisions that minimize the risk of the toxin being present in the fish. The recalled fish were not imported in compliance with those restrictions. FDA is examining all entries from the Chinese supplier and will take additional action, if warranted.

####

Firm Press Release (May 23, 2007)

FDA's Recalls, Market Withdrawals and Safety Alerts Page: http://www.fda.gov/opacom/7alerts.html

[GinaMarie]

Recall -- Firm Press Release


FDA posts press releases and other notices of recalls and market withdrawals from the firms involved as a service to consumers, the media, and other interested parties. FDA does not endorse either the product or the company. This listserv covers mainly Class I (life-threatening) recalls. A complete listing of recalls can be found in the FDA Enforcement Report at: http://www.fda.gov/opacom/Enforce.html

R.A.B. Food Group, LLC Issues a Nationwide Recall of Sparkling Grape Juices Product May Rupture
Contact:
David Rossi
201-417-4468

FOR IMMEDIATE RELEASE -- Secaucus, NJ -- May 24, 2007 – R.A.B. Food Group, LLC is recalling the following products

Manischewitz Sparkling Concord Grape Juice (UPC# 72700-05361) All Lot Codes
Manischewitz Sparkling Niagara Grape Juice (UPC# 72700-05362) All Lot Codes
Several bottles have been found to be fermenting which will cause additional pressure in the bottle. This may lead to the popping of the cap or rupturing of the bottle. There have been several incidents of rupturing bottles which could pose a hazard from broken glass. Immediate disposal of the product is warranted and should be done in a careful manner. There is no health risk posed from consuming the product and no consumer who has ingested the product is at any risk of illness or bad effects.

The recalled product has been distributed to retail stores throughout the United States and Canada.

Consumers that purchased any of the above products may contact R.A.B. Food Group, LLC for a full refund with proof of purchase. Consumers with questions about the recall or seeking a refund should call 1-201-453-5200.

####

FDA's Recalls, Market Withdrawals and Safety Alerts Page: http://www.fda.gov/opacom/7alerts.html

[GinaMarie]

Recall -- Firm Press Release


FDA posts press releases and other notices of recalls and market withdrawals from the firms involved as a service to consumers, the media, and other interested parties. FDA does not endorse either the product or the company. This listserv covers mainly Class I (life-threatening) recalls. A complete listing of recalls can be found in the FDA Enforcement Report at: http://www.fda.gov/opacom/Enforce.html



Whole Foods Market Issues Nationwide Recall of 365 Organic Everyday Value Sesame Tahini
Contact:
Kate Lowery
(512) 542-0390

FOR IMMEDIATE RELEASE -- Austin, TX -- May 22, 2007 - Whole Foods Market is voluntarily recalling 365 Organic Everyday Value Sesame Tahini 16-oz, with a Best By Date of 10/02/07 or earlier because it has the potential to be contaminated with Salmonella.

Food contaminated with Salmonella may not look or smell spoiled. Consumption of food contaminated with this bacteria may cause salmonellosis, a foodborne illness. In young children, the elderly and people with weakened immune systems, salmonellosis may cause serious and sometimes deadly infections. In otherwise healthy people, salmonellosis may cause short-term symptoms such as high fever, severe headache, vomiting, nausea, abdominal pain and diarrhea. Long-term complications may include severe arthritis.

365 Organic Everyday Value Sesame Tahini was distributed nationally through Whole Foods Market retail stores. The product comes in a 16-oz glass jar with the UPC number 0009948240599. The Best By Date is located on the top of the lid of the jar, any Best By Date of 10/02/07 or earlier is being recalled. No confirmed illnesses have been reported to date.

Potential salmonella contamination was brought to the attention of Whole Foods Market by the product's manufacturer. As a result, the company is voluntarily recalling this product as a precautionary measure and has put additional safety measures in place. No other Whole Foods Market Private Label products have been affected by this recall.

Consumers who have purchased 365 Organic Everyday Value Sesame Tahini can return it to Whole Foods Market for a full refund. Questions may be directed to the Company by calling (512) 477-5566 x20656 or via email at privatelabel.customerservice@wholefoods.com.

####

FDA's Recalls, Market Withdrawals and Safety Alerts Page: http://www.fda.gov/opacom/7alerts.html

[GinaMarie]

This listserv covers mainly Class I (life-threatening) recalls. A complete listing of recalls can be found in the FDA Enforcement Report at: http://www.fda.gov/opacom/Enforce.html



FOR IMMEDIATE RELEASE
P07-93
May 26, 2007

Media Inquiries:
Karen Riley, 301-827-6242
Consumer Inquiries:
888-INFO-FDA




Advanced Medical Optics Voluntarily Recalls Complete MoisturePlus Contact Lens Solution
The U.S. Food and Drug Administration is alerting health care professionals and their patients who wear soft contact lenses about a voluntary recall of Complete MoisturePlus Multi Purpose Solution manufactured by Advanced Medical Optics of Santa Ana, Ca.

The company is taking this action as a precaution because of reports of a rare, but serious, eye infection, Acanthamoeba keratitis, caused by a parasite. The link between the solution and the infection was identified as a result of an investigation by the Centers for Disease Control and Prevention (CDC).

Consumers who wear soft contact lenses should stop using the solution, discard all partially-used or unopened bottles and replace their lenses and storage container.

"We believe the company acted responsibly in taking this voluntary action and support their decision to be proactive in the interest of public health," said Daniel Schultz, M.D., director of FDA's Center for Devices and Radiological Health. "FDA and CDC are working closely with the company to collect additional information and we will continue to alert consumers and advise them as more information becomes available."

Acanthamoeba keratitis may lead to vision loss with some patients requiring a corneal transplant. The infection primarily affects otherwise healthy people who wear contact lenses.

Consumers should ask their doctor about choosing an appropriate alternative cleaning/disinfecting product and seek immediate treatment if they have symptoms of eye infection as early diagnosis is important for effective treatment. The symptoms of Acanthamoeba keratitis can be very similar to those of other more common eye infections and may include eye pain or redness, blurred vision, light sensitivity, sensation of something in the eye or excessive tearing but Acanthamoeba is more difficult to treat.

It is estimated that Acanthamoeba keratitis infections occur in approximately 2 out of every 1 million contact lens users in the United States each year. However, in a multi-state investigation to evaluate a recent increase in Acanthamoeba keratitis cases, CDC determined that the risk of developing AK was at least seven times greater for those consumers who used Complete MoisturePlus solution versus those who did not. Additional information regarding the CDC results is available at the CDC website http://www.cdc.gov/mmwr.

"The ongoing CDC investigation is a collaborative effort," said Michael Beach, M.D., a Division of Parasitic Diseases team leader with CDC. "We are working with FDA, state, territory, university, and clinical partners in an effort to further understand whether usage or contamination of this solution led to these Acanthamoeba infections."

All contact lens users should closely adhere to the following measures to help prevent eye infections:

Remove contact lenses before any activity involving contact with water, including showering, using a hot tub, or swimming.
Wash hands with soap and water and dry them before handling contact lenses.
Clean contact lenses according to manufacturer guidelines and instructions from an eye care professional.
Use fresh cleaning or disinfecting solution each time lenses are cleaned and stored. Never reuse or top off old solution.
Never use saline solution and rewetting drops to disinfect lenses. Neither solution is an effective or approved disinfectant.
Schedule regular eye exams with your eye care professional
Wear and replace contact lenses according to the schedule prescribed by your eye care professional.
Store lenses in a proper storage case.
Storage cases should be irrigated with sterile contact lens solution (never use tap water) and left open to dry after each use.
Replace storage cases at least once every three months.
FDA and CDC want to gather information related to Acanthamoeba keratitis in contact lens users. Report adverse events related to these products to MedWatch, the FDA's voluntary reporting program: www.fda.gov/medwatch/report.htm; Phone: (800) 332-1088; Fax: (800) 332-0178; Mail: MedWatch, Food and Drug Administration, 5600 Fishers Lane, Rockville, MD, 20852-9787.

Consumers who believe they are in possession of the recalled product may call the company at 1-888-899-9183.

Additional information about Acanthamoeba infection is available from the CDC website at http://www.cdc.gov/ncidod/dpd/parasites/acanthamoeba/index.htm.

####

FDA's Recalls, Market Withdrawals and Safety Alerts Page: http://www.fda.gov/opacom/7alerts.html

[GinaMarie]

Recall -- Firm Press Release


FDA posts press releases and other notices of recalls and market withdrawals from the firms involved as a service to consumers, the media, and other interested parties. FDA does not endorse either the product or the company. This listserv covers mainly Class I (life-threatening) recalls. A complete listing of recalls can be found in the FDA Enforcement Report at: http://www.fda.gov/opacom/Enforce.html



nSpired Natural Foods Issues Nationwide Recall of Maranatha Sesame Tahini Because of Possible Health Risk
Contact:
Lisa Wolford
646.805.2014

FOR IMMEDIATE RELEASE -- (San Leandro, CA, May 25, 2007) nSpired Natural Foods of San Leandro, California is voluntarily recalling all MaraNatha Sesame Tahini in 16-oz sizes with a Use By Date of 04/11/08 and earlier, and 15-lb and 32-lb sizes with an expiration date of 01/05/08 (lot 07130) and earlier, because it has the potential to be contaminated with Salmonella, an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Healthy persons infected with Salmonella often experience fever, diarrhea (which may be bloody), nausea, vomiting and abdominal pain. In rare circumstance, infection with Salmonella can result in the organism getting into the bloodstream and producing more severe illnesses such as arterial infections (i.e., infected aneurysms), endocarditis and arthritis.

MaraNatha Sesame Tahini was distributed nationally through distributors, retail stores, and mail order.

MaraNatha Sesame Tahini comes in a 16-oz glass jar, and 15-lb and 32-lb pails. Products affected are Organic Raw Sesame Tahini, Organic Roasted Sesame Tahini, Natural Raw Sesame Tahini and Natural Roasted Sesame Tahini.

There have been no confirmed cases of illness to date.

Potential salmonella contamination was discovered during routine, random sample testing by the Canadian Food Inspection Agency. As a result, the company is voluntarily recalling this product as a precautionary measure and has put additional safety measures in place. No other products produced by the company, which include Almond Butter, Peanut Butter, Cashew Butter and Macadamia Nut Butter, are affected by this action.

Consumers who have purchased MaraNatha Sesame Tahini are urged to return it to the place of purchase for a full refund. Consumers with questions may contact the company at 1-800-883-8312.

####

FDA's Recalls, Market Withdrawals and Safety Alerts Page: http://www.fda.gov/opacom/7alerts.html

[GinaMarie]

Recall -- Firm Press Release


FDA posts press releases and other notices of recalls and market withdrawals from the firms involved as a service to consumers, the media, and other interested parties. FDA does not endorse either the product or the company. This listserv covers mainly Class I (life-threatening) recalls. A complete listing of recalls can be found in the FDA Enforcement Report at: http://www.fda.gov/opacom/Enforce.html



Abbott Announces Voluntary Nationwide Recall of Three Lots of Two-Ounce Bottles of Similac Special Care 24 Cal / fl. oz. Ready-to-Feed (RTF) Premature Infant Formula with Iron
Contact:
Consumer Hotline
888-899-9182

FOR IMMEDIATE RELEASE -- Columbus, OH -- May 25, 2007 -- Abbott's Ross Products Division today announced a voluntary nationwide recall of three lots of two-ounce bottles of Similac Special Care 24 Cal / fl. oz. Ready-to-Feed (RTF) Premature Infant Formula with Iron, a highly specialized liquid ready-to-feed formula used only for premature infants after discharge from the hospital. This product is sold in eight unit cartons of two-ounce plastic bottles in the United States, and is primarily sold through pharmacies at the direction of a health care professional. It is not commonly available on retail store shelves.

Abbott is voluntarily recalling these three lots because they do not contain as much iron as indicated on the label. No serious medical complaints have been reported.

Premature infants fed this formula for more than a month after discharge could have an increased risk of developing anemia due to insufficient iron intake. If parents have any concerns about their baby's health, they should contact their baby's doctor or health care professional.

The recall is limited to stock code number 59582 with lot numbers 46815D5, 47847D5 or 52023D5 printed on the outside carton and case and the lot numbers 44427X8, 4427X81 or 50005X8 printed on the bottom of the bottles. No other liquid or powdered Similac infant formulas are affected.

The three lots of infant formula were distributed in the United States between November 2006 and May 2007. Consumers who purchased Similac Special Care 24 Cal / fl. oz. RTF Premature Infant Formula with Iron from any of the specific lots mentioned above should contact Abbott's Ross Products Division at 1-888-899-9182. Ross will replace product from these lots free of charge.

Similac Special Care 24 Cal / fl. oz. RTF Premature Infant Formula is a highly specialized formula used by premature infants for a limited amount of time after discharge from the hospital. The impacted product is not used in hospitals.

Abbott is working with the U.S. Food and Drug Administration and its distribution partners to execute this recall.

####

FDA's Recalls, Market Withdrawals and Safety Alerts Page: http://www.fda.gov/opacom/7alerts.html