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U.S. Department of Health and Human Services

Medical Device Recalls
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351 to 360 of 500 Results *
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Product Description
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Recall
Class
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FDA Recall
Posting Date
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Recalling Firm
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KinAir IV TheraPulse II AC-Powered Adjustable Hospital Beds 2 04/18/2003 FEI # 1625774
Kinetic Concepts, Inc
Guidant Multi-Link Vision Coronary Stent System Catalog Numbers: 30 different catalog numbers hav... 2 04/22/2003 FEI # 2024168
Guidant Corporation ACS
Custom surgical packs for a variety of surgical applications. Each pack is custom assembled and con... 2 04/22/2003 FEI # 1000125955
Windstone Medical, Inc.
RJ T&A PACK 2 04/22/2003 FEI # 1000125955
Windstone Medical, Inc.
T & A PACK 2 04/22/2003 FEI # 1000125955
Windstone Medical, Inc.
BACK PACK 2 04/22/2003 FEI # 1000125955
Windstone Medical, Inc.
ARTHROSCOPY PACK 2 04/22/2003 FEI # 1000125955
Windstone Medical, Inc.
CLOWARD PACK 2 04/22/2003 FEI # 1000125955
Windstone Medical, Inc.
DR. DESAI''S PACK 2 04/22/2003 FEI # 1000125955
Windstone Medical, Inc.
ABDOMINAL GYN PACK 2 04/22/2003 FEI # 1000125955
Windstone Medical, Inc.

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