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U.S. Department of Health and Human Services

Medical Device Recalls
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171 to 180 of 500 Results *
Recall Date to: 07/22/2014
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Product Description
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Recall
Class
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FDA Recall
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00597001131 Femur CR PRC SURF HDN FEM CO-NID AML, Rx, Sterile; ... 2 08/22/2013 Zimmer, Inc.
00597201101 Femur CR POROUS FEM COMP SIZE AML Rx, Sterile; 00597201102 Femur CR POROUS FEM COMP S... 2 08/22/2013 Zimmer, Inc.
65597201131 Femur CR POR FEM SURF HDN HATCP AML Rx, Sterile; 65597201132 Femur CR POR FEM SURF H... 2 08/22/2013 Zimmer, Inc.
00597201131 Femur CR POR SURF HDN FEM CO-NID AML Rx, Sterile; 00597201132 Femur CR POR SURF HDN F... 2 08/22/2013 Zimmer, Inc.
65597201101 Femur CR POR FEM HATCP SIZE AML Rx, Sterile; 65597201102 Femur CR POR FEM HATCP SIZ... 2 08/22/2013 Zimmer, Inc.
00597601201 Femur CRA PRECOAT FEM COMP SIZE B/L Rx, Sterile; 00597601202 Femur CRA PRECOAT FEM CO... 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.
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.

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