Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K032396 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Modular Head Component, Biomet Hip System; Item No. 11-363661, Hip Joint, metal/polymer/metal, semi-... | 2 | 04/27/2018 | Zimmer Biomet, Inc. |
36MM COCR MODULAR HD -6MM | 2 | 03/14/2018 | Zimmer Biomet, Inc. |
various polyethylene implants Hips Active Articulation ArComXL Bearings Active Articulation E1 B... | 2 | 03/27/2017 | Zimmer Biomet, Inc. |
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