Medical Device Recalls
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1 result found
510(K) Number: K954970 |
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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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| 20IN (50.8CM) BRAIDED INJ LINE, ROTATING ADAPT, List Number MX682BR | 2 | 01/17/2024 |
FEI # 1526863 Smiths Medical Asd Inc |
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