Medical Device Recalls
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81 to 83 of 83 Results
510(K) Number: K933785 |
Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Knee Stem Extensions & Impactor Sleeve: STEM IMPLANT 20MMDX145MM STEM IMPLANT 22MMDX145MM STEM IM... | 2 | 08/26/2014 | Zimmer, Inc. |
MODULAR CUP NEUTRAL LINER MODULAR CUP 10 DEGREE LIN MODULAR CUP 20 DEGREE LIN MODULAR CUP 7MM OFF... | 2 | 02/20/2014 | Zimmer, Inc. |
NexGen® Complete Knee Solutions Stemmed Tibial Component Precoat NexGen Tibial Baseplates are par... | 2 | 12/11/2013 | Zimmer, Inc. |
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