Medical Device Recalls
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1 result found
510(K) Number: K013527 |
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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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| RIA Tube Assembly, minimum 520 mm length, sterile- intended for use in adults and adolescents (12-2... | 2 | 03/01/2024 |
FEI # 3008812560 Synthes (USA) Products LLC |
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