Medical Device Recalls
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51 to 60 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-0803-2023 - PPM CLINICAL CRAPONNE CHROMID VRE 20 PLT US, CATALOG 43851 | 2 | 01/04/2023 |
FEI # 1950204 Biomerieux Inc |
| Z-0804-2023 - PPM CLINICAL CRAPONNE CHROMID C.DIFFICILE 20 PLT, CATALOG 43871 | 2 | 01/04/2023 |
FEI # 1950204 Biomerieux Inc |
| Z-0847-2023 - PPM CLINICAL CHROMID STREPTO B US 20 PLT, CATALOG 419751 | 2 | 01/04/2023 |
FEI # 1950204 Biomerieux Inc |
| Z-0842-2023 - PPM CLINICAL CHROMID MRSA S AUREUS 20PLT US, CATALOG 414524 | 2 | 01/04/2023 |
FEI # 1950204 Biomerieux Inc |
| Z-0802-2023 - PPM CLINICAL CHROMID MRSA 20 PLT US, CATALOG 43841 | 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-0840-2023 - GENE-UP REAGENT GENE-UP LYSIS KIT, CATALOG 414057 | 2 | 01/04/2023 |
FEI # 1950204 Biomerieux Inc |
| Z-0831-2023 - ETEST CLINICAL VANCOMYCIN VA 256 US S30, CATALOG 412486 | 2 | 01/04/2023 |
FEI # 1950204 Biomerieux Inc |
| Z-0830-2023 - ETEST CLINICAL TOBRAMYCIN TM 256 US S30, CATALOG 412478 | 2 | 01/04/2023 |
FEI # 1950204 Biomerieux Inc |
| Z-0829-2023 - ETEST CLINICAL RIFAMPICIN RI 32 US S30, CATALOG 412449 | 2 | 01/04/2023 |
FEI # 1950204 Biomerieux Inc |
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