Medical Device Recalls
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Related Medical Device Recalls |
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Product Description
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Recall
Class
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FDA Recall
Posting Date
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Recalling Firm
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| Z-0783-2023 - API LISTERIA 10 STRIPS+10 MEDIA, CATALOG 10300 | 2 | 01/04/2023 |
FEI # 1950204 Biomerieux Inc |
| Z-0784-2023 - API 20 E 25 STRIPS, CATALOG 20100 | 2 | 01/04/2023 |
FEI # 1950204 Biomerieux Inc |
| Z-0785-2023 - API 20 C AUX 25 STRIPS+25 MEDIA, CATALOG 20210 | 2 | 01/04/2023 |
FEI # 1950204 Biomerieux Inc |
| Z-0786-2023 - API STAPH 25 STRIPS+25 MEDIA, CATALOG 20500 | 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-0788-2023 - VITEK 2 REAGENT GP TEST KIT VTK2 20 CARDS, CATALOG 21342 | 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-0790-2023 - VITEK 2 REAGENT BCL TEST KIT VTK2 20 CARDS, CATALOG 21345 | 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-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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