Medical Device Recalls
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1 result found
510(K) Number: K872856 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| BioPro Femoral Head Product ID/Description 14089 HEAD FEMORAL 28 SH LT 14090 HEAD FEMORAL 28 M... | 2 | 10/14/2025 | BioPro, Inc. |
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