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U.S. Department of Health and Human Services

Medical Device Recalls
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51 to 60 of 94 Results
Related Medical Device Recalls
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Product Description
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Z-0833-2023 - VITEK 2 REAGENT AST-GN69 TEST KIT 20 CARDS, CATALOG 413400 2 01/04/2023 FEI # 1950204
Biomerieux Inc
Z-0834-2023 - VITEK 2 REAGENT AST-GN70 TEST KIT 20 CARDS, CATALOG 413401 2 01/04/2023 FEI # 1950204
Biomerieux Inc
Z-0835-2023 - VITEK 2 REAGENT AST-GN73 TEST KIT 20 CARDS, CATALOG 413404 2 01/04/2023 FEI # 1950204
Biomerieux Inc
Z-0836-2023 - VITEK 2 REAGENT AST-GN79 TEST KIT 20 CARDS, CATALOG 413436 2 01/04/2023 FEI # 1950204
Biomerieux Inc
Z-0837-2023 - VITEK 2 REAGENT AST-GN80 TEST KIT 20 CARDS, CATALOG 413437 2 01/04/2023 FEI # 1950204
Biomerieux Inc
Z-0838-2023 - VITEK 2 REAGENT AST-GN81 TEST KIT 20 CARDS, CATALOG 413438 2 01/04/2023 FEI # 1950204
Biomerieux Inc
Z-0839-2023 - PPM INDUSTRY COMBOURG CHROMID CARBA US 20 PLT, CATALOG 414012 2 01/04/2023 FEI # 1950204
Biomerieux Inc
Z-0840-2023 - GENE-UP REAGENT GENE-UP LYSIS KIT, CATALOG 414057 2 01/04/2023 FEI # 1950204
Biomerieux Inc
Z-0841-2023 - ETEST CLINICAL CEFTOLOZANE/TAZO C/T US S30, CATALOG 414445 2 01/04/2023 FEI # 1950204
Biomerieux Inc
Z-0842-2023 - PPM CLINICAL CHROMID MRSA S AUREUS 20PLT US, CATALOG 414524 2 01/04/2023 FEI # 1950204
Biomerieux Inc
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