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U.S. Department of Health and Human Services

Medical Device Recalls

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161 to 170 of 500 Results *
Recall Date to: 07/24/2014
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Product Description
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Recall
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FDA Recall
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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.
90595202017 Articular Surface XLPE CR ART SURF AE12/PUR 17, Rx, Sterile; 90595202020 Articular Su... 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.
90597002009 Articular Surface CR ART SURF 12/PURPLE 09MM, Rx, Sterile; 90597002010 Articular Surf... 2 08/22/2013 Zimmer, Inc.
00597202009 Articular Surface CR ART SURF 12/PURPLE 09, Rx, Sterile; 00597202010 Articular Surfac... 2 08/22/2013 Zimmer, Inc.
00597602010 Articular Surface AC ART SURF 12/PUR 10, Rx, Sterile; 00597602012 Articular Surface A... 2 08/22/2013 Zimmer, Inc.
00595203110 Articular Surface XLPE CR ART SURF 3,4/SYEL 10, Rx, Sterile; 00595203112 Articular Su... 2 08/22/2013 Zimmer, Inc.
90595203117 Articular Surface XLPE CR ART SURF AE34/STYEL 17, Rx, Sterile; 90595203120 Articular ... 2 08/22/2013 Zimmer, Inc.

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