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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 10 of 500 Results *
Recall Date to: 03%2F02%2F2014 Firm: DePuy
 
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Product Description
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FDA Recall
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ProVision Hytrel Elastomer Hood; product 5431-05-000. 2 07/23/2003 Depuy Orthopaedics, Inc.
ProVision Disposable Hood; product 5431-50-000 2 07/23/2003 Depuy Orthopaedics, Inc.
ProVision Barrier Universal Hood/Gown; product 5431-33-000 2 07/23/2003 Depuy Orthopaedics, Inc.
ProVision Hytrel Universal Hood/Gown; product 5431-31-000 2 07/23/2003 Depuy Orthopaedics, Inc.
Depuy brand ACE trochanteric nail lag screw; sterile, 80 mm; Product 903211080. 2 01/31/2004 Depuy Orthopaedics, Inc.
Depuy brand ACE trochanteric nail lag screw; sterile, 85 mm; Product 903211085. 2 01/31/2004 Depuy Orthopaedics, Inc.
Depuy brand ACE trochanteric nail lag screw; sterile, 90 mm; Product 903211090. 2 01/31/2004 Depuy Orthopaedics, Inc.
Depuy brand ACE trochanteric nail lag screw; sterile, 95 mm; Product 903211095. 2 01/31/2004 Depuy Orthopaedics, Inc.
Depuy brand ACE trochanteric nail lag screw; sterile, 100 mm; Product 903211100. 2 01/31/2004 Depuy Orthopaedics, Inc.
Depuy brand ACE trochanteric nail lag screw; sterile, 105 mm; Product 903211105. 2 01/31/2004 Depuy Orthopaedics, Inc.

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