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-0828-2023 - ETEST CLINICAL MINOCYCLINE MC 256 US S30, CATALOG 412407 | 2 | 01/04/2023 |
FEI # 1950204 Biomerieux Inc |
| Z-0827-2023 - ETEST CLINICAL MEROPENEM MP 32 US S30, CATALOG 412401 | 2 | 01/04/2023 |
FEI # 1950204 Biomerieux Inc |
| Z-0826-2023 - ETEST CLINICAL LEVOFLOXACIN LE 32 US S30, CATALOG 412392 | 2 | 01/04/2023 |
FEI # 1950204 Biomerieux Inc |
| Z-0849-2023 - ETEST CLINICAL IMIPENEM RELEBACTAM IPR US S30, CATALOG 420927 | 2 | 01/04/2023 |
FEI # 1950204 Biomerieux Inc |
| Z-0825-2023 - ETEST CLINICAL IMIPENEM IP 32 US S30, CATALOG 412373 | 2 | 01/04/2023 |
FEI # 1950204 Biomerieux Inc |
| Z-0824-2023 - ETEST CLINICAL FLUCONAZOLE FL 256 US S30, CATALOG 412333 | 2 | 01/04/2023 |
FEI # 1950204 Biomerieux Inc |
| Z-0860-2023 - ETEST CLINICAL ETEST VANCOMYCIN VA M100 US, CATALOG 423788 | 2 | 01/04/2023 |
FEI # 1950204 Biomerieux Inc |
| Z-0852-2023 - ETEST CLINICAL ETEST MEROPENEM/VABORBACTAM MEV US S30, CATALOG 421560 | 2 | 01/04/2023 |
FEI # 1950204 Biomerieux Inc |
| Z-0859-2023 - ETEST CLINICAL ETEST MEROPENEM MP M100 US, CATALOG 423786 | 2 | 01/04/2023 |
FEI # 1950204 Biomerieux Inc |
| Z-0823-2023 - ETEST CLINICAL ERYTHROMYCIN EM 256 US S30, CATALOG 412333 | 2 | 01/04/2023 |
FEI # 1950204 Biomerieux Inc |
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