Cordis Corporation announced today a nationwide voluntary recall of all lots of the CROSSOVER™ Sheath Introducer due to complaints about stretching or fracture of the sheath during use. The CROSSOVER™ Sheath Introducer is a product developed and manufactured by Thomas Medical Products, Inc., and distributed by Cordis
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Cordis Initiates Nationwide Recall of CROSSOVER™ Sheath Introducer
CONMED Corporation’s (Nasdaq: CNMD) CONMED Linvatec unit announced today a voluntary recall for certain model numbers of the PRO5 & PRO6 series battery handpieces manufactured prior to May 31, 2008, and certain lots of the MC5057 Universal Cable manufactured prior to December 1, 2006 used with certain of CONMED Linvatec’s electric powered handpieces.
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CONMED Corporation Announces Voluntary Recall of Certain Powered Surgical Instrument Products
Adams Extract and Spice, LLC. is announcing a voluntary recall of products because they have the potential to be contaminated with Salmonella. The products contain a specific lot of ground red pepper supplied by Van de Vries Spice Corporation, 9 Elkins Road, East Brunswick, New Jersey 08816
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Adams Extract & Spice, LLC Announces Recall Because of Possible Health Risk
New York State Agriculture Commissioner Patrick Hooker today alerted consumers that Tiffany Food Corporation, located at 1182 Flushing Ave, Brooklyn, New York is recalling “Bifeng Nong fu Shanzhuang” plum candy due to the presence of undeclared sulfites. People who have severe sensitivity to sulfites may run the risk of serious or life-threatening reactions if they consume this product.
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Undeclared Sulfites in “Bifeng Nong Fu Shanzhuang” Plum Candy
The U.S.
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FDA Approves Colchicine for Acute Gout, Mediterranean Fever
CareFusion Corporation, which is expected to become a public company following its planned spinoff from Cardinal Health, today issued the following update regarding its previously disclosed recall of the Alaris System: On June 12, 2009, the company sent an urgent Medical Device Recall Notification to customers of its Alaris® System addressing potential risks identified with the Alaris System.
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Carefusion Issues Update Regarding Previously Disclosed June 12, 2009 Recall of the Alaris®
FoodScience Corporation of Essex Junction, Vermont 05452 is voluntarily recalling a total of approximately 1,250 bottles of its Children’s Multi Vitamins…
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FoodScience Corporation Recalls Kid’s Multivitamin for label Error
At the request of the U.S. Food and Drug Administration, U.S. Marshals today seized more than $1.5 million worth of food products, including herbs and botanicals, stored under filthy conditions at the American Mercantile Corporation of Memphis, Tenn.
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FDA: More than $1.5 Million of Adulterated Food, Food Ingredients Seized