Medical Device Recalls
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1 result found
510(K) Number: K952466 |
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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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| Apo B Reagent, REF: OSR6143 | 3 | 05/23/2025 |
FEI # 1000206808 Beckman Coulter Ireland, Inc. |
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