Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K010363 |
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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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ETEST CLINICAL ETEST MEROPENEM MP M100 US, CATALOG 423786 | 2 | 01/04/2023 | Biomerieux Inc |
ETEST CLINICAL MEROPENEM MP 32 US S30, CATALOG 412401 | 2 | 01/04/2023 | Biomerieux Inc |
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