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U.S. Department of Health and Human Services

Medical Device Recalls

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371 to 380 of 500 Results *
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Product Description
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Recall
Class
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FDA Recall
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PENROSE ACE BANDAGE 2 04/22/2003 FEI # 1000125955
Windstone Medical, Inc.
SUBCLAVIAN PROCEDURE TRAY 2 04/22/2003 FEI # 1000125955
Windstone Medical, Inc.
ISOLATION GOWN PACK 2 04/22/2003 FEI # 1000125955
Windstone Medical, Inc.
VALVE ACCESSORY PACK 2 04/22/2003 FEI # 1000125955
Windstone Medical, Inc.
n/a 2 04/22/2003 FEI # 1000125955
Windstone Medical, Inc.
3M Attest Steam Pack 1276F (biological indicator of steam sterilization for use at hospitals) . 3 04/22/2003 FEI # 2110898
3m Health Care
N/A 3 04/22/2003 FEI # 2110898
3m Health Care
N/A 2 04/22/2003 FEI # 3002095335
Boston Scientific Scimed
Boston Scientific Scimed Radius 4.0 mm x 31 mm Self-Expanding Coronary Stent with Over-the-Wire De... 2 04/22/2003 FEI # 3002095335
Boston Scientific Scimed
Boston Scientific Scimed Radius Monorail 4.0 mm x 31 mm Stent Systems, Catalog Number H74917485400 2 04/22/2003 FEI # 3002095335
Boston Scientific Scimed

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