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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: 07/14/2014
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Product Description
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Recall
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FDA Recall
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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.
00597003109 Articular Surface CR ART SURF 34/STRIPE YEL 9, Rx, Sterile; 00597003110 Articular Sur... 2 08/22/2013 Zimmer, Inc.
90597003109 Articular Surface CR ART SURF 34/STR YEL 09MM, Rx, Sterile; 90597003110 Articular Sur... 2 08/22/2013 Zimmer, Inc.
00597203109 Articular Surface CR ART SURF 34/STRIPE YEL 09, Rx, Sterile; 00597203110 Articular Su... 2 08/22/2013 Zimmer, Inc.
00597603110 Articular Surface AC ART SURF 34/STRIPED YEL 10, Rx, Sterile; 00597603112 Articular S... 2 08/22/2013 Zimmer, Inc.
00595204110 Articular Surface XLPE CR ART SURF 5-6/STRGRN 10, Rx, Sterile; 00595204112 Articular ... 2 08/22/2013 Zimmer, Inc.
90595204117 Articular Surface XLPE CR ART SURF AE56/STGRN 17, Rx, Sterile; 90595204120 Articular ... 2 08/22/2013 Zimmer, Inc.

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