Recall Roundup

Monday, June 15, 2009

FDA Issues Public Health Advisory Regarding Levemir Insulin

The U.S. Food and Drug Administration has learned that some stolen vials of the long-acting insulin Levemir made by Novo Nordisk Inc. have reappeared and are being sold in the U.S. market. Three lots or a total of 129,000 vials of this product were stolen in all. These stolen insulin vials may not have been stored and handled properly and may be dangerous for patients to use.

The FDA has received one report of a patient who suffered an adverse event due to poor control of glucose levels after using a vial from one of these three lots.

The agency is advising patients who use Levemir insulin to:

1. Check your personal supply of insulin to determine if you have Levemir insulin from one of the following lots: XZF0036, XZF0037, and XZF0038. Patients can locate the lot number on the side of the box of insulin and also on the side of the vial.

2. Do not use your Levemir insulin if it is from one of these lots. Replace it with a vial of Levemir insulin from another lot. If you must switch to another brand of insulin for any reason, first contact your healthcare provider as another insulin product may require adjustments in dosing.

3. Always visually inspect your insulin before using it. Levemir is a clear and colorless solution.

4. Contact the Novo Nordisk Customer Care Center at 800-727-6500 for what to do with vials from these lots or if you have any other questions.

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Torres Hillsdale Country Cheese LLC Announces the Recall of all lots of Soft Mexican Cheeses due to Possible Listeria Contamination

Torres Hillsdale Country Cheese of Reading, Michigan announces the recall of all lots of various types of soft Mexican-style cheeses due to potential Listeria contamination. Consumption of food contaminated with Listeria monocytogenes can cause Listeriosis, an uncommon but potentially fatal disease. Listeriosis can cause high fever, severe headache, neck stiffness and nausea. Listeriosis can also cause miscarriages and stillbirths. The very young, the pregnant, the elderly and persons with compromised immune systems are the most susceptible to infection. People experiencing these problems should seek immediate medical attention.

A sample of queso fresco cheese, taken by an investigator from the U.S. Food and Drug Administration on May 26, 2009, was subsequently tested by an FDA laboratory and discovered to be contaminated with Listeria monocytogenes.

The products were distributed to retails stores and delis in the following states: Illinois, Indiana, Michigan, Georgia, Tennessee, Kentucky, North Carolina, South Carolina, Ohio and Wisconsin.

The products were sold under the name 'Aguas Calientes' as follows:

Product Unit Size
Queso Asadero 12 oz and 10 lb ball
Queso Oaxaca 10 lb ball
Queso Fresco 1 lb and 8 oz.
Queso Requeson 1 gallon pail and 3 gallon pail
Morral Adobera 3 lb packages

Packaging may also include a label with the name "Torres Hillsdale Country Cheese LLC". The recall encompasses all expiration dates.

No illnesses have been reported to date in connection with the recalled products.

Consumers and retailers are urged to return all unused recalled product to the manufacturer. Consumers with questions may contact Salvador Torres, Manager, Torres Hillsdale Country Cheese LLC at 517-368-5990, Monday through Friday between 7 a.m. and 3 p.m. EDT.

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Thursday, June 11, 2009

Six Reported Deaths Prompt Urgent Re-announcement of Blair Recall of Women's Chenille Robes

The U.S. Consumer Product Safety Commission (CPSC) and Blair LLC, of Warren, Pa., are re-announcing the voluntary recall by Blair of 162,000 women's full length Chenille Robes. Since the recall was originally announced in April 2009, Blair has received reports of six deaths due to the robes catching on fire. Five of the six victims were female, and all five were cooking at the time of the incidents. Three of the victims were in their 80s.

CPSC and Blair announced the recall for the robes after Blair learned of three robes catching on fire, including one report of second-degree burns. Blair was subsequently made aware of the fatalities after the recall was announced and after Blair had sent letters of the recall to consumers who purchased the robes.

The Women's Chenille Robes have the following item numbers: 3093111, 3093112, 3093113, 3093114, 3093115, and 3093116. The item number is identified on a label in the garment's neckline. The robe is a one-piece garment made of plush sculpted chenille, a shaped stand collar, and horizontal chenille front and back yolks and cuffs. The robe has a full-button front with seven matching button closures, long sleeves with self cuffs, a straight bottom with self hem, and two sideseam pockets. The robe's sewn in label states: "100% Cotton, RN 81700, Made in Pakistan".

The robes were sold in Blair catalogs and Web site, and Blair stores in Warren, Pa., Grove City, Pa., and Wilmington, Del., from January 2003 through March 2009 from about $20 to $40.

CPSC and Blair once again urge consumers to stop wearing the garments immediately and contact Blair LLC for information on returning the robe and to receive a refund or a $50 gift card for Blair merchandise. Contact Blair toll-free at (877) 392-7095 between 9 a.m. and 9 p.m. ET Monday through Saturday, visit the firm's Web site at www.blair.com/recall, or contact the firm by e-mail at blairproductrecall@blair.com

"CPSC urges all consumers to report any incidents or injuries involving consumer products, even after a recall has been announced," said Acting CPSC Chairman Thomas Moore. "Contact the CPSC so that we may help prevent tragic deaths or injuries like those that might be related to the Blair robes."

Wednesday, June 10, 2009

Children's Hooded Sweatshirts with Drawstrings Recalled by Winterbee Due To Strangulation Hazard

LaJobi Recalls Babi Italia Pinehurst and Bonavita Hudson Drop Side Cribs; Risk of Entrapment and Suffocation

The U.S. Consumer Product Safety Commission, in cooperation with the firm named below, today announced a voluntary recall of the following consumer product. Consumers should stop using recalled products immediately unless otherwise instructed.

Name of Product: Bonavita "Hudson" and Babi Italia "Pinehurst" Drop Side Cribs

Units: About 2,900

Importer: LaJobi Inc., of Cranbury, N.J.

Hazard: The lower spring pins on the footboard and headboard can pop out of the tracks located on the drop side causing the drop side to detach from the crib. When the drop side detaches, it creates a hazardous gap between the drop side and the crib mattress in which infants and toddlers can become entrapped and suffocate or fall from cribs.

Incidents/Injuries: CPSC and LaJobi have received a total of 33 reports of drop side detachment due to spring pin failure. In these reports, two children became entrapped and one child fell from cribs. Both entrapped children were freed by caregivers, one child was bruised.

Description: The recalled cribs are wood with a metal mattress support and have drop sides and were sold in a variety of finishes including cherry, espresso, natural, and white. Hudson and Pinehurst drop side cribs with production dates from December 2006 through August 2007 are included in the recall. The recalled cribs have the production date, product order (PO) number, item number, and color printed on a label attached to the footboard or headboard.

Sold at: Babi Italia Pinehurst drop side cribs were sold exclusively by Babies "R" Us. Bonavita Hudson drop side cribs were sold at Baby Basics, Beautiful Beginnings, and Buy Buy Baby stores and children's product stores nationwide for about $300. Cribs were sold from December 2006 through December 2007.

Manufactured in: China

Remedy: CPSC urges parents and caregivers to immediately stop using the recalled cribs and find an alternative, safe sleeping environment for their baby. LaJobi will provide professional technicians to perform in-home installations of a free retrofit hardware kit. Consumers should contact LaJobi to register for the free retrofit kit service.

Consumer Contact: For additional information, contact Lajobi toll-free at (866) 688-9009 anytime, or visit the firm's Web site at www.Lajobi.com

Note: This recall does not apply to the LaJobi crib models with straight pins on the headboard and footboard or non drop side cribs.

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LaJobi Recalls Bonavita "Cabana" Drop Side Cribs Due To Entrapment and Strangulation Hazards

The U.S. Consumer Product Safety Commission, in cooperation with the firm named below, today announced a voluntary recall of the following consumer product. Consumers should stop using recalled products immediately unless otherwise instructed.

Name of Product: Bonavita "Cabana" Drop Side Cribs

Units: About 2,000

Importer: LaJobi Inc., of Cranbury, N.J.

Hazard: The wooden crib slats can detach or break creating a gap, which can pose an entrapment and strangulation hazard to infants and toddlers.

Incidents/Injuries: LaJobi has received 16 incident reports of crib slat failures, including 10 reports of slats falling out of rails and 6 reports of slats breaking. No injuries have been reported.

Description: This recall involves Bonavita "Cabana" wooden drop side cribs with metal mattress supports. The cribs were manufactured from January 2006 through October 2008 and have production dates between 01 JAN 2006 and 31 OCT 2008. The model name, color, product order (PO) number, production date and other crib identifiers are printed on a label located on the inside bottom rail of the headboard or footboard. The cribs were sold in three finishes, antique white, classic cherry and montego brown. Cribs with other production dates are not affected by this recall.

Sold at: USA Baby, Beautiful Beginnings, Buy Buy Baby and other specialty stores nationwide from January 2006 through May 2009 for about $450.

Manufactured in: Vietnam

Remedy: CPSC urges parents and caregivers to immediately stop using the recalled cribs and find an alternative, safe sleeping environment for their baby. Consumers should contact LaJobi to receive replacement crib side rails.

Consumer Contact: For additional information, contact LaJobi toll-free at (866) 688-9009 anytime, or visit the firm's Web site at www.LaJobi.com

Tuesday, June 9, 2009

FDA Acts to Halt Marketing of Certain Unapproved Prescription Narcotic Drugs

Patients Still Have Access to Approved Narcotics for Pain Relief

The U.S. Food and Drug Administration today warned nine companies to stop manufacturing 14 unapproved narcotic drugs that are marketed in several dosage forms and are widely used to treat pain.

The FDA's warning letters notified the companies they may be subject to enforcement action if they do not stop manufacturing and distributing prescription unapproved products that include high concentrate morphine sulfate oral solutions and immediate release tablets containing morphine sulfate, hydromorphone or oxycodone. This action does not include oxycodone capsules.

Those companies receiving warning letters are Boehringer Ingelheim Roxane, Inc., Columbus, Ohio; Cody Laboratories, Inc., Cody, Wyoming; Glenmark Pharmaceuticals Inc., Mahwah, N.J.; Lannett Company, Inc., Philadelphia; Lehigh Valley Technologies, Inc., Allentown, Pa.; Mallinckrodt Inc. Pharmaceuticals Group, St. Louis; Physicians Total Care Inc., Tulsa, Okla.; Roxane Laboratories Inc., Columbus, Ohio; and Xanodyne Pharmaceuticals Inc., Newport, Ky.

The warning letters are part of the FDA's initiative on marketed unapproved drugs announced in June 2006. At that time, the agency published a compliance policy guide describing its risk-based enforcement approach against illegally marketed unapproved drugs.

"Consumers have a right to expect that their drugs meet the FDA's safety and effectiveness standards," said Janet Woodcock, M.D., director of the FDA's Center for Drug Evaluation and Research (CDER). "Doctors and patients are often unaware that not all drugs on the market are backed by FDA approval. It is a high priority for the FDA to remove these products from the market because they may be unsafe, ineffective, inappropriately labeled, or of poor quality."

Consumers who rely on narcotics for pain relief continue to have access to narcotic products that the agency has evaluated and determined to be safe and effective. The FDA has determined that removal of the unapproved narcotic products will not create a shortage for consumers.

Consumers who may be concerned that they are taking any of these products should refer to the FDA's Unapproved Drugs Web page, which includes a list of manufacturers of these products. These consumers should consult a health care professional for detailed guidance on treatment options.

"We will continue to take aggressive action against those firms that do not have the required FDA approval for their drugs," said Deborah M. Autor, J.D., director of CDER's Office of Compliance. "Today's warning letters are another demonstration of our commitment to remove illegal, unapproved drugs from the market."

Manufacturers have 60 days to stop manufacturing these products. Distributors have 90 days to stop shipping existing products. Previously manufactured products may still be found on pharmacy shelves for a short time.

To view copies of the Warning Letters, the names of the companies and their affected products, see the FDA's Unapproved Drugs Web page at: http://www.fda.gov/cder/drug/unapproved_drugs/enforcement.htm#narcotics

Information on FDA-approved drugs

Drugs Marketed in the United States That Do Not Have Required FDA Approval: http://www.fda.gov/cder/drug/unapproved_drugs

If you would like to hear a replay of the FDA's telebriefing on this issue, callers in the United States and Canada may dial 1-888-566-0502. International callers may dial 1-203-369-3058. The replay will be available until April 6, 2009 at 11:59 p.m. EDT.
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FDA Alerts Consumers to Recall of Certain Pistachios

FDA and California Inspectors Identify Salmonella

The FDA and the California Department of Public Health (CDPH) are investigating Salmonella contamination in pistachio products sold by Setton Pistachio of Terra Bella Inc, Calif. The company has stopped all distribution of processed pistachios and will issue a voluntary recall involving approximately 1 million pounds of its products. Because the pistachios were used as ingredients in a variety of foods, it is likely this recall will impact many products. In addition, the investigation at the company is ongoing and may lead to additional pistachio product recalls.
The contamination involves multiple strains of Salmonella. Salmonella can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Thus far, several illnesses have been reported by consumers that may be associated with the pistachios. It is not yet known whether any of the Salmonella strains found in the pistachio products are linked to an outbreak. The FDA is conducting genetic testing of the samples to pursue all links.

Until FDA is able to provide more information, consumers should not eat pistachios or food products containing them (such as pistachio bakery goods and pistachio ice cream) unless they can determine that the products do not contain pistachios from Setton Pistachio of Terra Bella, Inc. ("Setton").

FDA will provide a searchable database of affected products at http://www.fda.gov/pistachios/ and will continue to update the public.

FDA first learned of the problem on March 24, when it was informed by Kraft Foods that its Back To Nature Trail Mix was found to be contaminated with Salmonella. Kraft had identified the source of the contamination to be pistachios from Setton and conducted a recall.
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Raw Alfalfa Sprouts Linked to Salmonella Contamination

The U.S. Food and Drug Administration (FDA) and the Centers for Disease Control and Prevention (CDC) today recommended that consumers not eat raw alfalfa sprouts, including sprout blends containing alfalfa sprouts, until further notice because the product has been linked to Salmonella serotype Saintpaul contamination. Other types of sprouts have not been implicated at this time.

The investigation indicates that the problem may be linked to contamination of seeds for alfalfa sprouts. Because suspect lots of seeds may be sold around the country and may account for a large proportion of the alfalfa seeds currently being used by sprout growers, and cases of illness are spread across multiple states, FDA and CDC are issuing this general advisory.

FDA will work with the alfalfa sprout industry to help identify which seeds and alfalfa sprouts are not connected with this contamination, so that this advisory can be changed as quickly as possible.

CDC, FDA and six State and local authorities have associated this outbreak with eating raw alfalfa sprouts. Michigan, Minnesota, Pennsylvania, South Dakota, Utah, and West Virginia have reported 31 cases of illness with the outbreak strain of Salmonella Saintpaul to CDC. Most of those who became ill reported eating raw alfalfa sprouts. Some reported eating raw sprouts at restaurants; others reported purchasing the raw sprouts at the retail level.

The illnesses began in mid-March. Cases are still being reported, and possible cases are in various stages of laboratory testing, so illnesses may appear in other states. No deaths have been reported. The number of infected people may be higher than currently reported because some illnesses have not yet been confirmed with laboratory testing.

The CDC and FDA recommend at all times that persons at high risk for complications, such as the elderly, young children, and those with compromised immune systems, not eat raw sprouts because of the risk of contamination with Salmonella or other bacteria. Salmonella is an organism that can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Healthy individuals 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 meningitis and bone infections.

Initial investigation results trace the contaminated raw alfalfa sprouts to multiple sprout growers in multiple states. This suggests a potential problem with the seeds used, as well as the possible failure of the sprout growers involved to appropriately and consistently follow the FDA Sprout Guidance issued in 1999. The guidance recommends an effective seed disinfection treatment immediately before the start of sprouting (such as treating seed in 20,000 parts per million Calcium hypochlorite solution with agitation for 15 minutes) and regularly testing the water used for every batch of sprouts for Salmonella and E coli O157:H7 contamination.

This outbreak appears to be an extension of an earlier outbreak in 2009. In February and March, an outbreak of Salmonella Saintpaul infections occurred in Nebraska, South Dakota, Iowa, Kansas, and Minnesota. This outbreak was linked to raw alfalfa sprouts, and the outbreak strain was indistinguishable from that of these recently reported cases. A separate outbreak of Listeria monocytogenes infections was also linked to sprouts in 2009. In the 1990s, a number of outbreaks related to sprouts led FDA to issue its guidance. Experience over the past decade has shown that the likelihood of Salmonella in sprouts can be minimized when recommendations from FDA’s Sprout Guidance are followed.

Preventive controls are very important in the growing of all raw sprouts. FDA reminds sprout growers to be vigilant in their food safety practices and strongly encourages sprout growers to follow the Agency’s Sprout Guidance. Additionally, the United Fresh Produce Association has advised all of its members to follow FDA’s guidance on sprouts. FDA appreciates that the produce industry has reinforced this message and reminds retailers that it is prudent to sell sprouts from growers who follow FDA's recommendations.

For persons who continue to eat sprouts, visit (U.S. Food and Drug Administration, 2002 consumer advisory, available at http://www.cfsan.fda.gov/~lrd/tpsprout.html).
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Thursday, June 4, 2009

Children's Loungewear Recalled by Warm Biscuit Bedding Due to Violation of Federal Flammability Standards

The U.S. Consumer Product Safety Commission, in cooperation with the firm named below, today announced a voluntary recall of the following consumer product. Consumers should stop using recalled products immediately unless otherwise instructed.

Name of Product: Children's Loungewear Garments

Units: About 9,500

Distributer: Warm Biscuit Bedding Co., of New York, N.Y.

Hazard: The loungewear garments fail to meet children's sleepwear federal flammability standards which require sleepwear, including loungewear, to be either snug-fitting or flame resistant.

Incidents/Injuries: None reported.

Description: This recall involves loungewear sets for children described as "Lounge-Around-the-Housewear", "Lounge-About-Housewear" or "Short sets." The garments were sold in a variety of styles, colors and printed fabrics. They were sold in sizes S (1-2 yr), M (2-3 yr), L (3-4 yr), XL (4-5 yr), 6 yr, 7 yr and 8 yr. All of the garments have a label on the inside that says: "These garments do NOT comply with the Federal Flammability Standards and therefore are not suitable for sleepwear". The style numbers are 301101, 301102 and 301103 and are located on the packaging.

Sold by: Warm Biscuit Bedding catalogs and Web site from January 2000 through March 2009 for between $39 and $45.

Manufactured in: China and United States

Remedy: Consumers should stop using these children's loungewear garments immediately and contact Warm Biscuit Bedding to receive a store credit.

Consumer Contact: For additional information, contact Warm Biscuit Bedding at (800) 231-4231 between 9 a.m. and 6 p.m. ET Monday through Sunday or visit the firm's Web site at www.warmbiscuit.com. Consumers also can write to: Warm Biscuit Bedding Company, 140 Fulton Street, New York, NY 10038.

Wednesday, June 3, 2009

Hair Dryers Recalled by Vintage International Due to Electrocution Hazard

Bicycles Recalled by REI Due to Fork Failure

Bugaboo Recalls Strollers Due to Risk of Brake Failure

Tuesday, June 2, 2009

Nutro Products Announces Voluntary Recall of Limited Range of Dry Cat Food Products

Recently, Nutro Products announced a voluntary recall of select varieties of NUTRO® NATURAL CHOICE® COMPLETE CARE® Dry Cat Foods and NUTRO® MAX® Cat Dry Foods with “Best If Used By Dates” between May 12, 2010 and August 22, 2010. The cat food is being voluntarily recalled in the United States and ten additional countries. This recall is due to incorrect levels of zinc and potassium in our finished product resulting from a production error by a US-based premix supplier.

Two mineral premixes were affected. One premix contained excessive levels of zinc and under-supplemented potassium. The second premix under-supplemented potassium. Both zinc and potassium are essential nutrients for cats and are added as nutritional supplements to NUTRO® dry cat food.

This issue was identified during an audit of our documentation from the supplier. An extensive review confirmed that only these two premixes were affected. This recall does not affect any NUTRO® dog food products, wet dog or cat food, or dog and cat treats.

Affected product was distributed to retail customers in all 50 states, as well as to customers in Canada, Mexico, Japan, Korea, Thailand, Malaysia, Singapore, Indonesia, New Zealand, and Israel. We are working with all of our distributors and retail customers, in both the US and internationally, to ensure that the recalled products are not on store shelves. These products should not be sold or distributed further.

Consumers who have purchased affected product should immediately discontinue feeding the product to their cats, and switch to another product with a balanced nutritional profile. While we have received no consumer complaints related to this issue, cat owners should monitor their cat for symptoms, including a reduction in appetite or refusal of food, weight loss, vomiting or diarrhea. If your cat is experiencing health issues or is pregnant, please contact your veterinarian.

Consumers who have purchased product affected by this voluntary recall should return it to their retailer for a full refund or exchange for another NUTRO® dry cat food product. Cat owners who have questions about the recall should call 1-800-833-5330 between the hours 8:00 AM to 4:30 PM CST, or visit www.nutroproducts.com.

Recalled Pet Food

The varieties of NUTRO® NATURAL CHOICE® COMPLETE CARE® Dry Cat Foods and NUTRO® MAX® Cat Dry Foods listed below with “Best If Used By Dates” between May 12, 2010 and August 22, 2010 are affected by this voluntary recall.

Nutro Products Recall List – Dry Cat Foods

U.S. Product Name	Bag Size	UPC
NUTRO® NATURAL CHOICE® COMPLETE CARE® Kitten Food	4 lbs	0 79105 20607 5
NUTRO® NATURAL CHOICE® COMPLETE CARE® Kitten Food	8 lbs.	0 79105 20608 2
NUTRO® NATURAL CHOICE® COMPLETE CARE® Kitten Food (Bonus Bag)	9.2 lbs.	0 79105 20695 2
NUTRO® NATURAL CHOICE® COMPLETE CARE® Kitten Food	20 lbs	0 79105 20609 9
NUTRO® NATURAL CHOICE® COMPLETE CARE® Kitten Food (Sample Bag)	1.5 oz	none
NUTRO® NATURAL CHOICE® COMPLETE CARE® Adult	4 lbs	0 79105 20610 5
NUTRO® NATURAL CHOICE® COMPLETE CARE® Adult	8 lbs.	0 79105 20611 2
NUTRO® NATURAL CHOICE® COMPLETE CARE® Adult (Bonus Bag)	9.2 lbs	0 79105 20694 5
NUTRO® NATURAL CHOICE® COMPLETE CARE® Adult	20 lbs	0 79105 20612 9
NUTRO® NATURAL CHOICE® COMPLETE CARE® Adult (Sample Bag)	1.5 oz	none
NUTRO® NATURAL CHOICE® COMPLETE CARE® Adult Oceanfish Flavor	4 lbs	0 79105 20622 8
NUTRO® NATURAL CHOICE® COMPLETE CARE® Adult Oceanfish Flavor	8 lbs	0 79105 20623 5
NUTRO® NATURAL CHOICE® COMPLETE CARE® Adult Oceanfish Flavor (Bonus Bag)	9.2 lbs.	0 79105 20698 3
NUTRO® NATURAL CHOICE® COMPLETE CARE® Adult Oceanfish Flavor	20 lbs	0 79105 20624 2

NUTRO® MAX® Cat Adult Roasted Chicken Flavor	3 lbs	0 79105 10228 5
NUTRO® MAX® Cat Adult Roasted Chicken Flavor	6 lbs	0 79105 10229 2
NUTRO® MAX® Cat Adult Roasted Chicken Flavor	16 lbs	0 79105 10230 8
NUTRO® MAX® Cat Adult Roasted Chicken Flavor (Sample Bag)	1.5 oz	none
NUTRO® MAX® Cat Indoor Adult Roasted Chicken Flavor	3 lbs	0 79105 10243 8
NUTRO® MAX® Cat Indoor Adult Roasted Chicken Flavor	6 lbs	0 79105 10244 5
NUTRO® MAX® Cat Indoor Adult Roasted Chicken Flavor	16 lbs	0 79105 10245 2
NUTRO® MAX® Cat Indoor Adult Roasted Chicken Flavor (Sample Bag)	1.5 oz	none
NUTRO® MAX® Cat Indoor Adult Salmon Flavor	3 lbs	0 79105 10246 9
NUTRO® MAX® Cat Indoor Adult Salmon Flavor	6 lbs	0 79105 10247 6
NUTRO® MAX® Cat Indoor Adult Salmon Flavor	16 lbs	0 79105 10248 3
NUTRO® MAX® Cat Indoor Weight Control	3 lbs	0 79105 10249 0
NUTRO® MAX® Cat Indoor Weight Control	6 lbs	0 79105 10250 6
NUTRO® MAX® Cat Indoor Weight Control	16 lbs	0 79105 10251 3

LeClerc Foods Announces a Limited Nationwide Voluntary Recall of Market Pantry Chocolate Chip Chewy Granola Bars due to Unlabeled Peanut Allergen

Leclerc Foods has initiated a limited voluntary recall of a single lot of Market Pantry Chocolate Chip Chewy Granola Bar packages with UPC Code 85239 20124 and a “Best By” date of 18JAN2010.

The recall was initiated as a precautionary measure after it was discovered that product was mispackaged and the retail units may also contain Peanut Butter Chocolate Chip Bars and S’more Bars. As a result the ingredient statement on the retail package does not include peanuts as an ingredient. People who have allergies to peanuts run the risk of serious or life threatening allergic reactions if they consume this product.

The wrappers of the individual bars within the retail package have correct variety name on it. However, out of an abundance of precaution, the mispackaged product is being recalled.

No illnesses or allergic reactions have been reported to date.

The product is available in 15.2 oz. boxes containing 18 bars per box and the date code is found printed in white on the right side of the box. The “Best By” date of 18JAN2010 is the only date code affected by the recall. This product was distributed in Target stores in 35 states (AK, AL, CA, CO, CT, DC, DE, FL, GA, ID, IL, IN, MA, MD, ME, MI, MN, MO, MT, ND, NE, NH, NJ, NV, NY, OH, OR, PA RI, SC, UT, VA, WA WI, WY).

No other Market Pantry products are involved in this recall.

The safety and quality of Leclerc Foods USA, Inc. products are of utmost importance to the company.

Consumers are advised not to consume these items and may return the items to Target for a refund or they may call Target Guest Relations at 1-800-316-6151.

Consumers with additional questions on the recall may contact Leclerc Foods Customer Service at 1-800-463-6144, Monday to Friday between 8:30am and 4:30pm EDT.

This recall is being made with the knowledge of the Food and Drug Administration.

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