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 … [Read more...]
Expanded Voluntary Recall of Mazuri® Feed Products Due to Potential ElevatedVitamin 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 … [Read more...]
Pacific International Marketing Voluntarily Recalls 19 Cases of Bulk Romaine Lettuce Sold At Vons And Pavilions Stores In California And NevadaDue 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. The lettuce heads are banded with a red twist tie … [Read more...]
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". Whey protein is considered a derivative … [Read more...]
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. The corrective action … [Read more...]
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