Teva Animal Health, Inc. is expanding a nationwide voluntary recall of Ketamine Hydrochloride Injection, USP CIII 100mg/mL in 10mL vials for all lot numbers within their expiration dates to the Veterinary Level. This product had previously been recalled to the distributor level and is being expanded as a result of an increased trend in serious … [Read more...]

The Medicines Company (NASDAQ: MDCO) announced today that it is voluntarily recalling eleven (11) lots of Cleviprex ® (clevidipine butyrate) injectable emulsion due to the potential presence of visible particulate matter which has been observed in some vials during a routine annual inspection. The affected Cleviprex lots are 61-978-DW, 61-979-DW, … [Read more...]

Pompano Beach, FL – Atlas Operations, Inc. announced today that it is conducting a voluntary nationwide recall of the company's dietary supplements for sexual enhancement sold under Lot Numbers 494, 520C, 520B, 520A, 520, 521, 705, 706, 779 & 807. These products are currently being sold as a dietary supplement throughout the U.S. Atlas Operations, … [Read more...]

Recall Class: Class I Date Recall Initiated:  October 26, 2009 Product:  Operating Room System II Surgical Navigation Systems Product Name Stryker Catalog Number Serial#/Lot# Range Navigation System II-Cart 7700-100-000 Serial #s 100715-100735 PC SPC-1 Assembly 7700-101-201 Lot # K7P00F6000 These devices were manufactured … [Read more...]

In consultation with the U.S. Food and Drug Administration (FDA), Bayer’s Consumer Care division has begun a voluntary recall of a single product lot of the combination package of Alka-Seltzer Plus® Day & Night Cold Formula Liquid Gels. Bayer initiated the recall after identifying that the labeling on the foil blister card of certain packages … [Read more...]