Medical Device Recalls
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1 result found
510(K) Number: K051843 |
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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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Copeland HA Resurfacing Head, MB/HA EAS Head; Item Nos. 11-114641 11-114642 11-114643 11-114644 ... | 2 | 11/22/2019 | Zimmer Biomet, Inc. |
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