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...]

Recall Class: Class I Date Recall Initiated: October 21, 2009 Product: ViperSheath Sheath Introducer is manufactured by Thomas Medical Products, Inc. and is distributed by Cardiovascular Systems, Inc. (CSI). Lot Ranges Catalog Numbers S28117 through S29174 VPR-ISH 5 X 85, VPR-ISH 6 X 85, VPR-ISH 7 X 85, VPR-ISH 5 X 45, VPR-ISH 6 X 45, VPR-ISH 7 … [Read more...]

Stryker Corporation’s Instruments division initiated a worldwide, Class 1 recall of 23 Operating Room System II Surgical Navigation Systems because there is a potential for the navigation PC SPC-1 component to stop working which could result in the screen freezing, the system updating at a slow rate, or not responding at all. The potential harms … [Read more...]

The Procter & Gamble Company (NYSE:PG) announced today it is voluntarily recalling three lots of its Vicks Sinex nasal spray in three countries:  the United States, Germany and the United Kingdom. P&G said it is taking this precautionary step after finding the bacteria B. cepacia in a small amount of product made at its plant in Gross … [Read more...]