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U.S. Department of Health and Human Services

Medical Device Recalls
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31 to 40 of 500 Results *
Product: kne
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Product Description
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Recall
Class
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FDA Recall
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Recalling Firm
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00-5952-031-10, Nextgen Complete Knee System, Prolong highly crosslinked polyethylene Cruciate Retai... 2 05/14/2012 Zimmer Inc.
00-5970-020-09, NexGen CR Complete Knee Solution, Articular Surface regular constraint, Size Purple... 2 05/14/2012 Zimmer Inc.
00-5970-020-10, NexGen CR Complete Knee Solution, Articular Surface regular constraint, Size Purple... 2 05/14/2012 Zimmer Inc.
00-5970-020-12, NexGen CR Complete Knee Solution, Articular Surface regular constraint, Size Purple... 2 05/14/2012 Zimmer Inc.
00-5970-020-14, NexGen CR Complete Knee Solution, Articular Surface regular constraint, Size Purple... 2 05/14/2012 Zimmer Inc.
00-5970-020-17, NexGen CR Complete Knee Solution, Articular Surface regular constraint, Size Purple... 2 05/14/2012 Zimmer Inc.
00-5970-020-20 NexGen CR Complete Knee Solution, Cruciate Retaining (CR) Articular Surface Regular C... 2 05/14/2012 Zimmer Inc.
00-5970-02023, NexGen CompleteKnee Solution, Prolong, Highly Crosslinked Polyethylene Micro Articula... 2 05/14/2012 Zimmer Inc.
00-5972-020-09, NexGen CR Complete Knee Solution, Cruciate Retaining (CR) Articular Surface Regular ... 2 05/14/2012 Zimmer Inc.
00-5972-020-10, NexGen CR Complete Knee Solution, Cruciate Retaining (CR) Articular Surface Regular ... 2 05/14/2012 Zimmer Inc.

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