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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-0795-2023 - VIDAS CLINICALVIDAS VARICEL. ZOSTER IGG 60 T, CATALOG 30217 2 01/04/2023 FEI # 1950204
Biomerieux Inc
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-0853-2023 - VITEK 2 REAGENT AST-GN95 TEST KIT 20 CARDS, CATALOG 421982 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-0792-2023 - VITEK 2 REAGENT AST-GP67 TEST KIT 20 CARDS, CATALOG 22226 2 01/04/2023 FEI # 1950204
Biomerieux Inc
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