Cass-Clay Creamery of Fargo, N.D., is voluntarily recalling Hornbacher's Peppermint Bon Bon Light (half gallon/1.89 liter), Schroeder Peppermint Bon Bon (1.75 quart/1.65 liter) and SunnyBrook Peppermint Bon Bon Light (half gallon/1.89 liter) because they may contain undeclared eggs. People who have an allergy or severe sensitivity to eggs run the risk of serious or life-threatening allergic reaction if they consume these products.
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Expanded Voluntary Recall of Mazuri® Feed Products Due to Potential Elevated Vitamin D Level
PMI Nutrition International is expanding a voluntary recall to include three additional varieties of the Mazuri feed products listed below, due to the potential for an elevated vitamin D level in these products. Elevated vitamin D levels can be harmful to animals if fed for extended periods, and may result in lack of interest in eating, weight loss and possible joint stiffness.
FDA approves genetic test to help some colon cancer patients, physicians considering Erbitux therapy
The U.S. Food and Drug Administration today approved the first genetic test that can help some colorectal cancer (CRC) patients and their doctors determine if the drug Erbitux (cetuximab) would be an effective treatment based on the presence of a gene mutation.
Pacific International Marketing Voluntarily Recalls 19 Cases of Bulk Romaine Lettuce Sold At Vons And Pavilions Stores In California And Nevada Due To Possible Salmonella Contamination
Pacific International Marketing (“Pacific”) is voluntarily recalling 19 cases of bulk Romaine Lettuce sold at Vons and Pavilions stores in California and Nevada due to potential Salmonella contamination. The bulk Romaine Lettuce was sold in bulk produce bins from July 2, 2012 through July 4, 2012.
Arctic Zero Inc. Voluntarily Recalls For Relabeling Frozen Dessert Due To Undeclared Milk Allergen On Label.
Arctic Zero Inc. of Escondido, Ca. is voluntarily recalling to relabel pints and chocolate dipped bars which were produced before February of 2012, due to undeclared milk allergen. All products that were produced after February 2012 have the statement “Contains whey protein, which is a derivative of dairy”.
MAQUET Initiates Class I Recall of the FLOW-i Anesthesia System
Maquet Critical Care AB and MAQUET Medical Systems USA today issued the following update regarding its voluntary worldwide field correction for its C20, C30 and C40 FLOW-i Anesthesia Systems. The recall was related to a software problem with the MAN/AUTO switch used for changing between manual and automatic ventilation modes.
CDFA Announces Recall Of Andante Dairy Cheese
Multiple lots of cheeses made by Andante Dairy in Petaluma, California are the subject of a recall and quarantine order announced by California State Veterinarian Dr. Annette Whiteford. The quarantine is based on a determination that a lack of proper pasteurization could have allowed dangerous pathogens to survive in the products.
BI-LO Issues Class II Recall On Southern Home Brand Bacon Ranch Salad Mix & Creamy Parmesan Salad Mix
Today BI-LO announced an immediate Class II voluntary recall of two store brand products, the Southern Home Bacon Ranch Salad Mix and the Southern Home Creamy Parmesan Salad Mix. According to the Food & Drug Administration (FDA), the reason for the recall is the potential for the product to contain small metal fragments.
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FDA approves first DNA test to help manage CMV infection in organ transplant patients
The U.S. Food and Drug Administration today approved the first DNA test to help health care professionals gauge the progress of anti-viral treatment in solid organ transplant patients undergoing cytomegalovirus (CMV) antiviral therapy.
FDA prompts companies to remove certain unapproved oxycodone products from market
The U.S. Food and Drug Administration today issued a Federal Register notice instructing companies to stop manufacturing and distributing certain unapproved drugs that contain oxycodone. The notice is part of the FDA’s Unapproved Drugs Initiative to remove unapproved new drugs from the market.