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U.S. Department of Health and Human Services

Medical Device Recalls
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181 to 190 of 500 Results *
Recall Date to: 07/14/2014
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Product Description
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FDA Recall
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00597503110 Provisional AC ARTSURF PROV 34/STRIPE YEL10, Rx, Sterile; 00597503112 Provisional A... 2 08/22/2013 Zimmer, Inc.
00597504110 Provisional AC ART SURF PROV 56/STR GRN 10, Rx, Sterile; 00597504112 Provisional AC... 2 08/22/2013 Zimmer, Inc.
00597102010 Provisional CR ART SURF PROV 12/PURPLE 10, Rx, Sterile; 00597102012 Provisional CR ... 2 08/22/2013 Zimmer, Inc.
00597103110 Provisional CR ART SURF PROV 34/STR YEL 10, Rx, Sterile; 00597103112 Provisional CR... 2 08/22/2013 Zimmer, Inc.
00597104110 Provisional CR ART SURF PROV 56/STR GRN 10, Rx, Sterile; 00597104112 Provisional CR... 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.
00597206126 Patella ALL POLY PAT COMP MICRO 26DIA, Rx, Sterile; 00597206129 Patella ALL POLY PAT ... 2 08/22/2013 Zimmer, Inc.
00595202010 Articular Surface XLPE CR ART SURF 1,2/PUR 10, Rx, Sterile; 00595202012 Articular Sur... 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.

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