Medical Device Recalls
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1 result found
510(K) Number: K100544 |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| IMPIX DLIF, REF numbers: a) B16123509, b) B16123511, c) B16124009, d) B16124013, e) B161... | 2 | 08/24/2023 | Medicrea International |
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