Medical Device Recalls
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11 to 16 of 16 Results
510(K) Number: K090596 |
Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Zimmer Natural Nail System, Antegrade Femoral Recon Module, standard, nonsterile, Zimmer, Warsaw, IN... | 2 | 11/24/2009 | Zimmer Inc. |
Zimmer Natural Nail System, Antegrade Femoral Recon Module, small, nonsterile, Zimmer, Warsaw, IN; R... | 2 | 11/24/2009 | Zimmer Inc. |
Zimmer Natural Nail System, Antegrade Femoral Interlock Module, standard, nonsterile, Zimmer, Warsaw... | 2 | 11/24/2009 | Zimmer Inc. |
Zimmer Natural Nail System, Antegrade Femoral Interlock Module, small, nonsterile, Zimmer, Warsaw, I... | 2 | 11/24/2009 | Zimmer Inc. |
Various fixation systems and accessories, Item Nos. 00118100522 00118100527 00118100530 001181005... | 2 | 11/07/2019 | Zimmer Biomet, Inc. |
Triathlon PKR Peg Drill, Catalog Number: 5650-4-512 (Size 1-2 Peg Drill); Catalog Number: 5650-4-536... | 2 | 03/28/2011 | Stryker Howmedica Osteonics Corp. |
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