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U.S. Department of Health and Human Services

Medical Device Recalls

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510(K) Number: K983136
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Product is an Orthopedic device contained in a Peel Foil Pouch. Product is labeled in part: ''REF C... 2 09/21/2005 Linvatec Corp.
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 3 Packaging: The product was packaged within inner and outer blister trays, sealed wi... 2 06/29/2012 DePuy Orthopaedics, Inc.
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 5 Packaging: The product was packaged within inner and outer blister trays, sealed ... 2 06/29/2012 DePuy Orthopaedics, Inc.
LUSTER HIP SZ 6 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 8 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.
LUSTER HIP SZ 4 Packaging: The product was packaged within inner and outer blister trays, sealed ... 2 06/29/2012 DePuy Orthopaedics, Inc.
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