FDA Press Releases Archives - Page 720 of 816

Performance Plus Marketing Recalls Libigrow, Libigrow XXXtreme, Blue Diamond, Blue Diamond Platinum, Mojo Nights, Mojo Nights Supreme, Casanova Supplements

January 17, 2013 By The FDA Leave a Comment

Performance Plus Marketing, Inc. is recalling Libigrow®, Libigrow XXXtreme®, Blue Diamond®, Blue Diamond Platinum®, Mojo Nights®, Mojo Nights Supreme®, and Casanova® because they contain undeclared Sulfoaildenafil and Thioaildenafil. Performance Plus Marketing, Inc. has been informed by the US Food and Drug Administration (FDA) that FDA lab … [Read more...]

P&J Trading Recalls All Lots of the Dietary Supplements Slimdia Revolution

January 17, 2013 By The FDA Leave a Comment

P&J TRADING is conducting a voluntary nationwide recall of their dietary supplements sold under the brand name SLIMDIA REVOLUTION specific to the following product below. There is no identifying lot number. SLIMDIA REVOLUTION (bottles 30 capsules) P&J TRADING is conducting a voluntary recall after being notified by the US FDA that testing … [Read more...]

Praxair, Inc. Recalls Grab ‘n Go Vantage Portable Oxygen Cylinder Units

January 17, 2013 By The FDA Leave a Comment

Praxair, Inc. is in the process of conducting a voluntary recall involving Grab 'n Go Vantage portable oxygen cylinder units. Praxair is making a minor modification to the affected units as they come in for routine servicing and filling. Praxair has already communicated with its customers and the FDA. Praxair initiated this field correction after … [Read more...]

Qualitest Pharmaceuticals Recall: Three Lots of Hydrocodone Bitartrate and Acetaminophen Tablets, USP 10 mg/500 mg Distributed by Mylan Institutional

January 17, 2013 By The FDA Leave a Comment

Mylan Inc. announced that its Mylan Institutional business is recalling three lots of Hydrocodone Bitartrate and Acetaminophen Tablets, USP 10 mg/500 mg (Lots 3037841, 3040859 and 3042573). The three lots were manufactured by Qualitest Pharmaceuticals, and Mylan Institutional repackaged and distributed the product in unit dose (CD100) under the UDL … [Read more...]

Zimmer Spine Issues Urgent Worldwide Medical Device Recall Of The Inserter Instrument For The PEEK Ardis Interbody Spacer

January 17, 2013 By The FDA Leave a Comment

Zimmer Spine, Inc. is initiating a voluntary worldwide recall of all 315 units of the PEEK Ardis® Inserter. The Ardis Inserter is a surgical instrument used during spinal surgery to implant the PEEK Ardis Interbody Spacer. The inserters are being recalled because Zimmer Spine has received reports of PEEK Ardis Interbody Spacer implant breakage when … [Read more...]