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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 10 of 500 Results *
Recall Date to: 12/17/2014
 
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FDA Recall
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(Siemens Rad Fluoro Uro Systems) Ysio, Luminos Agile, Luminos dRF, and Uroskop Omnia systems with s... 2 11/26/2013 Siemens Medical Solutions USA, Inc
00-5952-31-12, Nextgen Complete Knee System, Prolong highly crosslinked polyethylene Cruciate Retai... 2 05/14/2012 Zimmer Inc.
00-5970-031-23, Nextgen Complete Knee System, Prolong highly crosslinked polyethylene Cruciate Reta... 2 05/14/2012 Zimmer Inc.
00-5972-031-23, Nextgen Complete Knee System, Prolong highly crosslinked polyethylene Cruciate Reta... 2 05/14/2012 Zimmer Inc.
00-5976-031-10, Nextgen Complete Knee System, Prolong highly crosslinked polyethylene Cruciate Reta... 2 05/14/2012 Zimmer Inc.
00-5976-031-12, Nextgen Complete Knee System, Prolong highly crosslinked polyethylene Cruciate Reta... 2 05/14/2012 Zimmer Inc.
00-5976-031-14, Nextgen Complete Knee System, Prolong highly crosslinked polyethylene Cruciate Reta... 2 05/14/2012 Zimmer Inc.
00-5976-031-17, Nextgen Complete Knee System, Prolong highly crosslinked polyethylene Cruciate Reta... 2 05/14/2012 Zimmer Inc.
00-5976-031-20, Nextgen Complete Knee System, Prolong highly crosslinked polyethylene Cruciate Reta... 2 05/14/2012 Zimmer Inc.
00-5976-031-23, Nextgen Complete Knee System, Prolong highly crosslinked polyethylene Cruciate Reta... 2 05/14/2012 Zimmer Inc.

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