Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K933549 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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VIDAS CMV IgM, 30 tests, REF 30205-01, IVD, Rx. | 2 | 03/14/2022 | bioMerieux, Inc. |
VIDAS® CMV IgM 30 Tests | 2 | 04/10/2021 | Biomerieux Inc |
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