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U.S. Department of Health and Human Services

Medical Device Recalls
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11 to 20 of 94 Results
Related Medical Device Recalls
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Z-0848-2023 - VITEK 2 REAGENT AST-ST02 TEST KIT 20 CARDS, CATALOG 420915 2 01/04/2023 FEI # 1950204
Biomerieux Inc
Z-0856-2023 - VITEK 2 REAGENT AST-N801 TEST KIT 20 CARDS, CATALOG 423416 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-0843-2023 - VITEK 2 REAGENT AST-GP75 TEST KIT 20 CARDS, CATALOG 415670 2 01/04/2023 FEI # 1950204
Biomerieux Inc
Z-0792-2023 - VITEK 2 REAGENT AST-GP67 TEST KIT 20 CARDS, CATALOG 22226 2 01/04/2023 FEI # 1950204
Biomerieux Inc
Z-0854-2023 - VITEK 2 REAGENT AST-GN99 TEST KIT 20 CARDS, CATALOG 423102 2 01/04/2023 FEI # 1950204
Biomerieux Inc
Z-0853-2023 - VITEK 2 REAGENT AST-GN95 TEST KIT 20 CARDS, CATALOG 421982 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-0837-2023 - VITEK 2 REAGENT AST-GN80 TEST KIT 20 CARDS, CATALOG 413437 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
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