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U.S. Department of Health and Human Services

Medical Device Recalls

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1 to 3 of 3 Results
510(K) Number: K070292
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Product Description
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FDA Recall
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Metasul® Durom® Femoral component Sterile, Rx 2 11/06/2012 Zimmer, Inc.
Zimmer Durom Hip Resurfacing Systems, Femoral Component 54 Code T; Catalog No.: 01.00211.154, Zimmer... 2 11/29/2007 Zimmer Inc.
Zimmer Durom Hip Resurfacing Systems, Femoral Component 46 Code L; Catalog No.: 01.00211.146, Lot 23... 2 11/29/2007 Zimmer Inc.
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