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U.S. Department of Health and Human Services

Medical Device Recalls
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61 to 70 of 94 Results
Related Medical Device Recalls
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Product Description
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FDA Recall
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Z-0828-2023 - ETEST CLINICAL MINOCYCLINE MC 256 US S30, CATALOG 412407 2 01/04/2023 Biomerieux Inc
Z-0827-2023 - ETEST CLINICAL MEROPENEM MP 32 US S30, CATALOG 412401 2 01/04/2023 Biomerieux Inc
Z-0826-2023 - ETEST CLINICAL LEVOFLOXACIN LE 32 US S30, CATALOG 412392 2 01/04/2023 Biomerieux Inc
Z-0849-2023 - ETEST CLINICAL IMIPENEM RELEBACTAM IPR US S30, CATALOG 420927 2 01/04/2023 Biomerieux Inc
Z-0825-2023 - ETEST CLINICAL IMIPENEM IP 32 US S30, CATALOG 412373 2 01/04/2023 Biomerieux Inc
Z-0824-2023 - ETEST CLINICAL FLUCONAZOLE FL 256 US S30, CATALOG 412333 2 01/04/2023 Biomerieux Inc
Z-0860-2023 - ETEST CLINICAL ETEST VANCOMYCIN VA M100 US, CATALOG 423788 2 01/04/2023 Biomerieux Inc
Z-0852-2023 - ETEST CLINICAL ETEST MEROPENEM/VABORBACTAM MEV US S30, CATALOG 421560 2 01/04/2023 Biomerieux Inc
Z-0859-2023 - ETEST CLINICAL ETEST MEROPENEM MP M100 US, CATALOG 423786 2 01/04/2023 Biomerieux Inc
Z-0823-2023 - ETEST CLINICAL ERYTHROMYCIN EM 256 US S30, CATALOG 412333 2 01/04/2023 Biomerieux Inc
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