Medical Device Recalls
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1 result found
510(K) Number: K853250 |
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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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FEMOROTIBIAL/FEMORAL NAIL, various sizes. Item Nos. 32855331111 32855331113 32855331115 328553311... | 2 | 11/07/2019 | Zimmer Biomet, Inc. |
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