Medical Device Recalls
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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-0843-2023 - VITEK 2 REAGENT AST-GP75 TEST KIT 20 CARDS, CATALOG 415670 | 2 | 01/04/2023 |
FEI # 1950204 Biomerieux Inc |
| Z-0844-2023 - PPM LOMBARD PRODUCTS IRR COUNT-TACT 3P AGAR 100 PLT, CATALOG 418049 | 2 | 01/04/2023 |
FEI # 1950204 Biomerieux Inc |
| Z-0845-2023 - PPM LOMBARD PRODUCTS TSA 3P W NEUTRALIZERS 100 PLT, CATALOG 419014 | 2 | 01/04/2023 |
FEI # 1950204 Biomerieux Inc |
| Z-0846-2023 - ETEST CLINICAL CEFTAZIDIM/AVIBACTAM US S30, CATALOG 419046 | 2 | 01/04/2023 |
FEI # 1950204 Biomerieux Inc |
| Z-0847-2023 - PPM CLINICAL CHROMID STREPTO B US 20 PLT, CATALOG 419751 | 2 | 01/04/2023 |
FEI # 1950204 Biomerieux Inc |
| Z-0848-2023 - VITEK 2 REAGENT AST-ST02 TEST KIT 20 CARDS, CATALOG 420915 | 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-0850-2023 - VITEK 2 REAGENT AST-GP78 TEST KIT 20 CARDS, CATALOG 421051 | 2 | 01/04/2023 |
FEI # 1950204 Biomerieux Inc |
| Z-0851-2023 - ETEST CLINICAL ERAVACYCLINE ERV US S30, CATALOG 421553 | 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 |
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