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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 10 of 94 Results
Related Medical Device Recalls
 
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Z-0816-2023 - VITEK MS CLINICAL REAGENT VITEK MS-FA, CATALOG 411072 2 01/04/2023 FEI # 1950204
Biomerieux Inc
Z-0814-2023 - VITEK MS CLINICAL REAGENT VITEK MS-DS, CATALOG 410893 2 01/04/2023 FEI # 1950204
Biomerieux Inc
Z-0815-2023 - VITEK MS CLINICAL REAGENT VITEK MS-CHCA, CATALOG 411071 2 01/04/2023 FEI # 1950204
Biomerieux Inc
Z-0789-2023 - VITEK 2 REAGENT YST TEST KIT VTK2 20 CARDS, CATALOG 21343 2 01/04/2023 FEI # 1950204
Biomerieux Inc
Z-0791-2023 - VITEK 2 REAGENT NH TEST KIT VTK2 20 CARDS, CATALOG 21346 2 01/04/2023 FEI # 1950204
Biomerieux Inc
Z-0788-2023 - VITEK 2 REAGENT GP TEST KIT VTK2 20 CARDS, CATALOG 21342 2 01/04/2023 FEI # 1950204
Biomerieux Inc
Z-0787-2023 - VITEK 2 REAGENT GN TEST KIT VTK2 20 CARDS, CATALOG 21341 2 01/04/2023 FEI # 1950204
Biomerieux Inc
Z-0790-2023 - VITEK 2 REAGENT BCL TEST KIT VTK2 20 CARDS, CATALOG 21345 2 01/04/2023 FEI # 1950204
Biomerieux Inc
Z-0861-2023 - VITEK 2 REAGENT AST-XN15 TEST KIT 20 CARDS, CATALOG 423829 2 01/04/2023 FEI # 1950204
Biomerieux Inc
Z-0857-2023 - VITEK 2 REAGENT AST-XN09 TEST KIT 20 CARDS, CATALOG 423425 2 01/04/2023 FEI # 1950204
Biomerieux Inc
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