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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 10 of 276 Results
Product: arn Recall Date to: 10/09/2014
 
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ISPAN patient bracelet, given to patients post surgery to warn of further use of dinitrogen monoxide 2 12/17/2003 Alcon Laboratories, Inc
Kallestad (TM) HEp-2 Cell Line Substrate. Product labeled "BIO-RAD Kallestad (TM) HEp-2 Cell Line S... 3 09/19/2008 Bio-Rad Laboratories
Kallestad (TM) Mouse Stomach/Kidney, catalog number 30443 - 8 wells, 48 tests. Product labeled "BIO... 3 09/19/2008 Bio-Rad Laboratories
Kallestad (TM) Mouse Kidney. Product labeled "BIO-RAD Kallestad (TM) Mouse Kidney Substrate... UNIT... 3 09/19/2008 Bio-Rad Laboratories
The SternaLock Blu Implant Tray includes plates, screws, screw measuring device, and blades. The... 2 01/24/2012 Biomet Microfixation, Inc.
The LactoSorb Heat/Contouring Pen is a disposable alkaline-battery powered device. Product is lab... 2 03/27/2012 Biomet Microfixation, LLC
Oxford Femoral Knee System REF 154600, LOT 2272736, WARNING DO NOT RESTERILIZE, STERILE UNLESS PACK ... 2 06/29/2011 Biomet U.K., Ltd.
CircuCool Fluid Circulation Pump used in the Chilli Cooled Ablation System, Model Number M00480050, ... 2 03/17/2010 Boston Scientific Corp
Boston Scientific, IMAGER II Angiographic Catheter, Sterilized with ethylene oxide gas. Made in Irel... 2 04/11/2012 Boston Scientific Corporation
Cardinal Health Custom Sterile Latex Free Convenience Kits; sterile single use disposable devices pa... 2 11/18/2005 Cardinal Health
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