Medical Device Recalls
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1 result found
510(K) Number: K934068 |
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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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| Direct Bilirubin Reagents (DBIL 2 x 200 ) and (DBIL 2 x 300), Ref:439715 (200 tests/cartridge) and 4... | 2 | 03/02/2020 |
FEI # 2050010 Beckman Coulter Inc |
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