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U.S. Department of Health and Human Services

Medical Device Recalls
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21 to 30 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-0821-2023 - ETEST CLINICAL CEFTRIAXONE TX 32 US S30, CATALOG 412302 2 01/04/2023 Biomerieux Inc
Z-0863-2023 - ETEST CLINICAL COLISTIN CO 256 US B100, CATALOG 537348 2 01/04/2023 Biomerieux Inc
Z-0851-2023 - ETEST CLINICAL ERAVACYCLINE ERV US S30, CATALOG 421553 2 01/04/2023 Biomerieux Inc
Z-0822-2023 - ETEST CLINICAL ERTAPENEM ETP 32 US S30, CATALOG 412331 2 01/04/2023 Biomerieux Inc
Z-0823-2023 - ETEST CLINICAL ERYTHROMYCIN EM 256 US S30, CATALOG 412333 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-0852-2023 - ETEST CLINICAL ETEST MEROPENEM/VABORBACTAM MEV US S30, CATALOG 421560 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-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
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