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U.S. Department of Health and Human Services

Medical Device Recalls
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191 to 200 of 500 Results *
Recall Date to: 01/27/2015
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Product Description
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FDA Recall
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NexGen Complete Knee Solution Porous Patella Drill Guide-26mm dia./10mm thickness Non sterile, Rx ... 2 12/06/2013 Zimmer, Inc.
Trinica Anterior Lumbar Plate (ALP) system, part 07.01058.001. Non Sterile, Rx only. The Trinica An... 2 11/18/2013 Zimmer, Inc.
VerSys® Cemented Revision Calcar (CRC) Hip System Femoral Stems VerSys Heritage Hip System Revision... 2 11/14/2013 Zimmer, Inc.
Ti-Magna Fx Washer Ti-Versa-FX®II Femoral Fixation System S/C Plates The compression tube/plat... 2 11/01/2013 Zimmer, Inc.
CoCr Head (Not distributed in the United States) Used in total hip replacement. 2 10/25/2013 Zimmer, Inc.
Sidus" Head (Not distributed in the United States) 2 10/25/2013 Zimmer, Inc.
NexGen CR-Flex Mobile Bearing Tibial Component 9 (Not distributed in the United States) 2 10/25/2013 Zimmer, Inc.
Natural-Knee® II Femoral Component 2 10/25/2013 Zimmer, Inc.
Gender Solutions" Patello-Femoral Component 2 10/25/2013 Zimmer, Inc.
Zimmer® Unicompartmental Knee Femoral Component. Indicated for patients with painful and/or disab... 2 10/25/2013 Zimmer, Inc.

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