Medical Device Recalls
-
|
31 to 40 of 94 Results
Related Medical Device Recalls |
Results per Page |
|
Product Description
![Sort by Product Name [A-Z]](/scripts/cdrh/images/arrow_up-black.GIF){kind=icon} ![Sort by Product Name [Z-A]](/scripts/cdrh/images/arrow_down-black.GIF){kind=icon}
|
Recall
Class
|
FDA Recall
Posting Date
|
Recalling Firm
|
|---|---|---|---|
| Z-0849-2023 - ETEST CLINICAL IMIPENEM RELEBACTAM IPR US S30, CATALOG 420927 | 2 | 01/04/2023 |
FEI # 1950204 Biomerieux Inc |
| Z-0826-2023 - ETEST CLINICAL LEVOFLOXACIN LE 32 US S30, CATALOG 412392 | 2 | 01/04/2023 |
FEI # 1950204 Biomerieux Inc |
| Z-0827-2023 - ETEST CLINICAL MEROPENEM MP 32 US S30, CATALOG 412401 | 2 | 01/04/2023 |
FEI # 1950204 Biomerieux Inc |
| Z-0828-2023 - ETEST CLINICAL MINOCYCLINE MC 256 US S30, CATALOG 412407 | 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 |
| Z-0830-2023 - ETEST CLINICAL TOBRAMYCIN TM 256 US S30, CATALOG 412478 | 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-0840-2023 - GENE-UP REAGENT GENE-UP LYSIS KIT, CATALOG 414057 | 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-0802-2023 - PPM CLINICAL CHROMID MRSA 20 PLT US, CATALOG 43841 | 2 | 01/04/2023 |
FEI # 1950204 Biomerieux Inc |
-
