Winn-Dixie today announced an immediate Class II voluntary recall of Winn-Dixie Cheeseburger Macaroni Skillet Dinners sold in the 5.8 oz. package with a UPC code of 2114018080, and a sell-by date of May 14, 2013. 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 introduces new safety measures for extended-release and long-acting opioid medications
The U.S. Food and Drug Administration today approved a risk evaluation and mitigation strategy (REMS) for extended-release (ER) and long-acting (LA) opioids, highly potent drugs approved for moderate to severe, persistent pain that requires treatment for an extended period.
Sedona Labs Issues A Voluntary Recall For iFlora Kids Multi-Probiotic And iFlora 4-Kids Powder Dietary Supplements Due To Possible Health Risk
Sedona Labs today announced that its supplier of Galactooligosaccharide (GOS) has recalled this ingredient due to a possible Salmonella contamination. As a result, we are now voluntarily recalling certain lots of our iFlora Kids Multi-Probiotic and iFlora 4-Kids Powder distributed between 3/16/2011 and 5/3/2012.
Stryker Initiates Voluntary Product Recall of Modular-Neck Stems Action Specific to Rejuvenate and ABG II Modular-Neck Stems
Stryker has voluntarily recalled its Rejuvenate and ABG II modular-neck stems. “While modular-neck stems provide surgeons with an option to correct certain aspects of a patient’s anatomy and hip biomechanics, given the potential risks associated with fretting and corrosion at the modular neck junction, Stryker Orthopaedics decided to take this voluntary action,” said Stuart Simpson, Vice President and General Manager, Hip Reconstruction.
Cass-Clay Creamery Issues Allergy Alert on Undeclared Eggs in Peppermint Bon Bon Ice Cream
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.
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.