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U.S. Department of Health and Human Services

Medical Device Recalls
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Product Description
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Recall
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FDA Recall
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Belos VR - implantable cardioverter defibrillator. Implantable Cardioverter Defibrillators. The Be... 2 05/14/2003 FEI # 1028232
Biotronik Inc
CoaguChek Plus meter; catalog # 475729 and 12816001. 2 05/14/2003 FEI # 1823260
Roche Diagnostics Corp.
CoaguChek Pro DM meter; catalog # 1894048 and 1893211. 2 05/14/2003 FEI # 1823260
Roche Diagnostics Corp.
Mauch XG, Caron Knee Frame. Model numbers FDM01804U, FRM01804LU, FRM01851U, FRM61750. 2 05/14/2003 FEI # 1000519909
Ossur North America Inc
Twister(tm) Cube Back-Cane Short, a wheelchair back seat support strap, part number WPHS. 2 05/14/2003 FEI # 1181047
Action Products Incorporated
Polyflex Esophageal Stent 25/21mm x 120mm 2 05/14/2003 FEI # 3001451463
Boston Scientific Corporation
Polyflex Esophageal Stent 25/21mm x 150mm 2 05/14/2003 FEI # 3001451463
Boston Scientific Corporation
Polyflex Esophageal Stent 25/21mm x 90mm 2 05/14/2003 FEI # 3001451463
Boston Scientific Corporation
Polyflex Esophageal Stent 23/18mm x 150mm 2 05/14/2003 FEI # 3001451463
Boston Scientific Corporation
Polyflex Esophageal Stent 23/18mm x 120mm 2 05/14/2003 FEI # 3001451463
Boston Scientific Corporation

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