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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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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.
00595001201 Femur CR-FLEX PCT FEM B-L Rx, Sterile; 00595001202 Femur ... 2 08/22/2013 Zimmer, Inc.
00595201201 Femur CR-FLEX POR FEM B-L Rx, Sterile; 00595201202 Femur CR-FLEX POR FEM B-R Rx, St... 2 08/22/2013 Zimmer, Inc.
65595201201 Femur CR-FLEX POR HATCP FEM B-L Rx, Sterile; 65595201202 ... 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.
00597201303 Femur CR POR FM COMP SIZE CML Rx, Sterile; 00597201304 Femur CR POR FM COMP SIZE CMR... 2 08/22/2013 Zimmer, Inc.
00597201333 Femur CR POR SURF HDN FEM CO-NID CML, Rx, Sterile; 00597201334 Femur CR POR SURF HDN ... 2 08/22/2013 Zimmer, Inc.
65597201333 Femur CR POR FEM SURF HDN HATCP CML, Rx, Sterile; 65597201334 Femur CR POR FEM SURF H... 2 08/22/2013 Zimmer, Inc.
00587806126 Patella MICRO POROUS PAT 26MM X 10MM, Rx, Sterile; 00587806129 Patella MICRO POROUS P... 2 08/22/2013 Zimmer, Inc.

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