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U.S. Department of Health and Human Services

Medical Device Recalls
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181 to 190 of 500 Results *
Recall Date to: 09/01/2014
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Product Description
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FDA Recall
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e-fix E19 power drive. The product is a wheelchair component/accessory. 2 05/06/2005 Frank Mobility Systems, Inc.
dsDNA IgG ELISA 96 Well Kit, Catalog Number: DD037G The products in question are all Enzyme Linke... 2 03/05/2010 Calbiotech Inc
djo surgical Screw 6.5 mm, Sz 25mm, low profile. Product is intended for the fixation of the acet... 2 08/06/2012 Encore Medical, Lp
directCHECK Whole Blood Control; for Hemochron J. Microcoagulation Systems. 2 06/11/2010 International Technidyne Corporation
dideco Preassembled Surgical Wash Set, Electa Essential , Cobe part numbers WS55E, WS125E, WS175E, ... 2 09/09/2006 Cobe Cardiovascular, Inc
dideco Preassembled Surgical Wash Set, Compact , Cobe part numbers WS55C, WS125C, WS225C, Cobe Card... 2 09/09/2006 Cobe Cardiovascular, Inc
diaDexus PLAC Test ELISA Kit; Manufactured and distributed by diaDexus , Inc., South San Francisco, ... 2 11/22/2010 DiaDexus, Inc
diaDexus PLAC Test ELISA Kit, Enzyme Immunoassay for Quantitative Determination of Lp-PLA2 in human ... 2 03/21/2011 DiaDexus, Inc
diaDexus Inc. PLAC Test Reagent Kit, Turbidimetric Immunoassay for the Quantitative Determination of... 2 04/01/2009 DiaDexus, Inc
delete. created in error 3 01/23/2003 Roche Diagnostics Corp.

*   The maximium 500 devices meeting your search criteria returned. Please narrow your search.
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