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U.S. Department of Health and Human Services

Medical Device Recalls
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71 to 80 of 94 Results
Related Medical Device Recalls
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Z-0853-2023 - VITEK 2 REAGENT AST-GN95 TEST KIT 20 CARDS, CATALOG 421982 2 01/04/2023 Biomerieux Inc
Z-0854-2023 - VITEK 2 REAGENT AST-GN99 TEST KIT 20 CARDS, CATALOG 423102 2 01/04/2023 Biomerieux Inc
Z-0855-2023 - GENE-UP REAGENT GENE-UP Salmonella 2, CATALOG 423105 2 01/04/2023 Biomerieux Inc
Z-0856-2023 - VITEK 2 REAGENT AST-N801 TEST KIT 20 CARDS, CATALOG 423416 2 01/04/2023 Biomerieux Inc
Z-0857-2023 - VITEK 2 REAGENT AST-XN09 TEST KIT 20 CARDS, CATALOG 423425 2 01/04/2023 Biomerieux Inc
Z-0858-2023 - PPM LOMBARD PRODUCTS TSA 3P W NEUTRALIZERS 100 PLT, CATALOG 423723 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-0860-2023 - ETEST CLINICAL ETEST VANCOMYCIN VA M100 US, CATALOG 423788 2 01/04/2023 Biomerieux Inc
Z-0861-2023 - VITEK 2 REAGENT AST-XN15 TEST KIT 20 CARDS, CATALOG 423829 2 01/04/2023 Biomerieux Inc
Z-0862-2023 - ASTUTE REAGENT NEPHROCHECK LIQUID CONTROLS KIT US, CATALOG 500013 2 01/04/2023 Biomerieux Inc
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