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U.S. Department of Health and Human Services

Medical Device Recalls
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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.
00595202010 Articular Surface XLPE CR ART SURF 1,2/PUR 10, Rx, Sterile; 00595202012 Articular Sur... 2 08/22/2013 Zimmer, Inc.
00595202010, NexGen CompleteKnee Solution, Prolong, Highly CrossLinked Polyethylene Micro Articular ... 2 05/14/2012 Zimmer Inc.
00595202012, NexGen CompleteKnee Solution, Prolong, Highly CrossLinked Polyethylene Micro Articular ... 2 05/14/2012 Zimmer Inc.
00595202014, NexGen CompleteKnee Solution, Prolong, Highly CrossLinked Polyethylene Micro Articular ... 2 05/14/2012 Zimmer Inc.
00595202017, NexGen CompleteKnee Solution, Prolong, Highly CrossLinked Polyethylene Micro Articular ... 2 05/14/2012 Zimmer Inc.
00595202020, NexGen CompleteKnee Solution, Prolong, Highly Crosslinked Polyethylene Micro Articular ... 2 05/14/2012 Zimmer Inc.
00595203110 Articular Surface XLPE CR ART SURF 3,4/SYEL 10, Rx, Sterile; 00595203112 Articular Su... 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.

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