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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: 07/14/2014
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Product Description
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Recall
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FDA Recall
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00597004109 Articular Surface CR ART SURF 56/STRIPE GREEN 9, Rx, Sterile; 00597004110 Articular S... 2 08/22/2013 Zimmer, Inc.
90597004109 Articular Surface CR ART SURF AE56/STR GRN 09MM, Rx, Sterile; 90597004110 Articular S... 2 08/22/2013 Zimmer, Inc.
00597204109 Articular Surface CR ART SURF 56/STRIPE GRN 9, Rx, Sterile; 00597204110 Articular Sur... 2 08/22/2013 Zimmer, Inc.
00597604110 Articular Surface AC ART SURF 56/STRIPED GRN 10, Rx, Sterile; 00597604112 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.
00595501201 Provisional CR-FLEX FEM PROV SZ B-L, Rx, Sterile; 00595501202 Provisional CR-FLEX F... 2 08/22/2013 Zimmer, Inc.
00598706201 Provisional CRA FEM PROV/CUT GDE SZ BML, Rx, Sterile; 00598706202 Provisional CRA F... 2 08/22/2013 Zimmer, Inc.
00597106126 Provisional ALL POLY PAT PROV MICRO SZ 26, Rx, Sterile; 00597106129 Provisional ALL... 2 08/22/2013 Zimmer, Inc.
00597106126 Provisional MIC POROUS PAT PROV 26MMX10MM, Rx, Sterile; 00597106129 Provisional MIC... 2 08/22/2013 Zimmer, Inc.
00597502010 Provisional AC ART SURF PROV 12/PUR 10, Rx, Sterile; 00597502012 Provisional AC ART... 2 08/22/2013 Zimmer, Inc.

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