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U.S. Department of Health and Human Services

Medical Device Recalls
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41 to 50 of 94 Results
Related Medical Device Recalls
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Product Description
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Recall
Class
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FDA Recall
Posting Date
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Recalling Firm
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Z-0823-2023 - ETEST CLINICAL ERYTHROMYCIN EM 256 US S30, CATALOG 412333 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-0825-2023 - ETEST CLINICAL IMIPENEM IP 32 US S30, CATALOG 412373 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-0827-2023 - ETEST CLINICAL MEROPENEM MP 32 US S30, CATALOG 412401 2 01/04/2023 Biomerieux Inc
Z-0828-2023 - ETEST CLINICAL MINOCYCLINE MC 256 US S30, CATALOG 412407 2 01/04/2023 Biomerieux Inc
Z-0829-2023 - ETEST CLINICAL RIFAMPICIN RI 32 US S30, CATALOG 412449 2 01/04/2023 Biomerieux Inc
Z-0830-2023 - ETEST CLINICAL TOBRAMYCIN TM 256 US S30, CATALOG 412478 2 01/04/2023 Biomerieux Inc
Z-0831-2023 - ETEST CLINICAL VANCOMYCIN VA 256 US S30, CATALOG 412486 2 01/04/2023 Biomerieux Inc
Z-0832-2023 - BIOBALL K.RHIZOPHILA (30X20), CATALOG 412690 2 01/04/2023 Biomerieux Inc
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