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U.S. Department of Health and Human Services

Medical Device Recalls
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Product Description
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Recall
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00595501201 Provisional CR-FLEX FEM PROV SZ B-L, Rx, Sterile; 00595501202 Provisional CR-FLEX F... 2 08/22/2013 Zimmer, Inc.
00595601201 Femur CR-FLEX OPT FEM B-L Rx Sterile; 00595601202 Femur CR-FLEX OPT FEM B-R Rx Ste... 2 08/22/2013 Zimmer, Inc.
00597001101 Femur CR PRECOAT FEM COMP SIZE AML, Rx, Sterile; ... 2 08/22/2013 Zimmer, Inc.
00597001131 Femur CR PRC SURF HDN FEM CO-NID AML, Rx, Sterile; ... 2 08/22/2013 Zimmer, Inc.
00597001303 Femur CR PRC FEM COMP SIZE CML Rx, Sterile; 00597001304 Femur CR PRC FEM COMP SIZE ... 2 08/22/2013 Zimmer, Inc.
00597001333 Femur CR PRC SURF HDN FEM CO-NID CML Rx, Sterile; 00597001334 Femur CR PRC SURF HDN ... 2 08/22/2013 Zimmer, Inc.
00597002009 Articular Surface CR ART SURF 12/PURPLE 9, Rx, Sterile; 00597002010 Articular Surface... 2 08/22/2013 Zimmer, Inc.
00597003109 Articular Surface CR ART SURF 34/STRIPE YEL 9, Rx, Sterile; 00597003110 Articular Sur... 2 08/22/2013 Zimmer, Inc.
00597004109 Articular Surface CR ART SURF 56/STRIPE GREEN 9, Rx, Sterile; 00597004110 Articular S... 2 08/22/2013 Zimmer, Inc.
00597101101 Provisional CR PROV FRM COMP SIZE AML, Rx, Sterile; 00597101102 Provisional CR PROV... 2 08/22/2013 Zimmer, Inc.

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