Medical Device Recalls
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71 to 80 of 94 Results
Related Medical Device Recalls |
Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| 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-0855-2023 - GENE-UP REAGENT GENE-UP Salmonella 2, CATALOG 423105 | 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-0857-2023 - VITEK 2 REAGENT AST-XN09 TEST KIT 20 CARDS, CATALOG 423425 | 2 | 01/04/2023 |
FEI # 1950204 Biomerieux Inc |
| Z-0858-2023 - PPM LOMBARD PRODUCTS TSA 3P W NEUTRALIZERS 100 PLT, CATALOG 423723 | 2 | 01/04/2023 |
FEI # 1950204 Biomerieux Inc |
| Z-0859-2023 - ETEST CLINICAL ETEST MEROPENEM MP M100 US, CATALOG 423786 | 2 | 01/04/2023 |
FEI # 1950204 Biomerieux Inc |
| Z-0860-2023 - ETEST CLINICAL ETEST VANCOMYCIN VA M100 US, CATALOG 423788 | 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-0862-2023 - ASTUTE REAGENT NEPHROCHECK LIQUID CONTROLS KIT US, CATALOG 500013 | 2 | 01/04/2023 |
FEI # 1950204 Biomerieux Inc |
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