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U.S. Department of Health and Human Services

Medical Device Recalls
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101 to 110 of 500 Results *
Recall Date to: 03/02/2014 Firm: DePuy
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LUSTER HIP SZ 10 Packaging: The product was packaged within inner and outer blister trays, sealed... 2 06/29/2012 DePuy Orthopaedics, Inc.
LUSTER HIP SZ 9 Packaging: The product was packaged within inner and outer blister trays, sealed ... 2 06/29/2012 DePuy Orthopaedics, Inc.
LUSTER HIP SZ 8 Packaging: The product was packaged within inner and outer blister trays, sealed ... 2 06/29/2012 DePuy Orthopaedics, Inc.
LUSTER HIP SZ 7 Packaging: The product was packaged within inner and outer blister trays, sealed ... 2 06/29/2012 DePuy Orthopaedics, Inc.
LUSTER HIP SZ 5 Packaging: The product was packaged within inner and outer blister trays, sealed ... 2 06/29/2012 DePuy Orthopaedics, Inc.
LUSTER HIP SZ 4 Packaging: The product was packaged within inner and outer blister trays, sealed ... 2 06/29/2012 DePuy Orthopaedics, Inc.
LUSTER HIP SZ 3 Packaging: The product was packaged within inner and outer blister trays, sealed wi... 2 06/29/2012 DePuy Orthopaedics, Inc.
LUSTER HIP SZ 2 Packaging: The product was packaged within inner and outer blister trays, sealed ... 2 06/29/2012 DePuy Orthopaedics, Inc.
LUSTER HIP SZ 1 Packaging: The product was packaged within inner and outer blister trays, sealed ... 2 06/29/2012 DePuy Orthopaedics, Inc.
ULTIMA*LX STM,POL 10/12TAP/4M Packaging: The product was packaged within inner and outer PETG bli... 2 06/29/2012 DePuy Orthopaedics, Inc.

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