Jea R. Gackowski, Encompass Group Corporate Compliance Officer announced today the company is voluntarily recalling the Thermoflect product line for relabeling regarding its use in the MR (Magnetic Resonance) environment. "We are voluntarily recalling the product line from use in the Magnetic Resonance (MR) environment," Gackowski said. "We are … [Read more...]

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...]