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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-0783-2023 - API LISTERIA 10 STRIPS+10 MEDIA, CATALOG 10300 2 01/04/2023 Biomerieux Inc
Z-0784-2023 - API 20 E 25 STRIPS, CATALOG 20100 2 01/04/2023 Biomerieux Inc
Z-0785-2023 - API 20 C AUX 25 STRIPS+25 MEDIA, CATALOG 20210 2 01/04/2023 Biomerieux Inc
Z-0786-2023 - API STAPH 25 STRIPS+25 MEDIA, CATALOG 20500 2 01/04/2023 Biomerieux Inc
Z-0787-2023 - VITEK 2 REAGENT GN TEST KIT VTK2 20 CARDS, CATALOG 21341 2 01/04/2023 Biomerieux Inc
Z-0788-2023 - VITEK 2 REAGENT GP TEST KIT VTK2 20 CARDS, CATALOG 21342 2 01/04/2023 Biomerieux Inc
Z-0789-2023 - VITEK 2 REAGENT YST TEST KIT VTK2 20 CARDS, CATALOG 21343 2 01/04/2023 Biomerieux Inc
Z-0790-2023 - VITEK 2 REAGENT BCL TEST KIT VTK2 20 CARDS, CATALOG 21345 2 01/04/2023 Biomerieux Inc
Z-0791-2023 - VITEK 2 REAGENT NH TEST KIT VTK2 20 CARDS, CATALOG 21346 2 01/04/2023 Biomerieux Inc
Z-0792-2023 - VITEK 2 REAGENT AST-GP67 TEST KIT 20 CARDS, CATALOG 22226 2 01/04/2023 Biomerieux Inc
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