Medical Device Recalls
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1 result found
510(K) Number: K954808 |
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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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| Surgipro Monofilament Polypropylene Sutures Product Description CP-535 SURGIPRO* 1 BLU 100CM GS24 ... | 2 | 02/25/2023 |
FEI # 1219930 Covidien, LP |
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