Becton Dickinson & Co. Recall 93789
Description: BD BBL Sensi Disc Cefpodoxime - 10 ug, used for semi-quantitative in vitro susceptibility testing. Catalog Number 231673 and 231674¿
Becton Dickinson & Co. Recall 93789 Information
| Status | Ongoing |
| Mandated? | Voluntary: Firm initiated |
| Recall Number | Z-1021-2024 |
| Event ID | 93789 |
| Event Description | BD BBL Sensi Disc Cefpodoxime - 10 ug, used for semi-quantitative in vitro susceptibility testing. Catalog Number 231673 and 231674¿ |
| Product Type | Devices |
| Distribution | Domestic distribution nationwide. International distribution worldwide. |
| Quantity | 2,363,168 total units |
| Recall Reason | There is a possibility of reproducibility, accuracy, and/or QC failures in antibiotic susceptibility testing (AST) for H. influenzae. This may cause product discard, delayed results, or additional adverse diagnostic outcomes, such as a delay in diagnosis, the selection of inappropriate antibiotics, or extended duration of antibiotic exposure and the treatment process. |
| Device Classification | 20240214 |
| Device Code Info | Catalog No. 231673 UDI-DI 00382902316732 Lots 3109152 3157106 3241174; Catalog No. 231674 UDI-DI 30382902316740 Lots 3157106 3241174 3109152 |
| Center Classification Date | 20240208 |
| Recall Initiation Date | 20240108 |
| Recalling Firm | Becton Dickinson & Co. |
| Initial Notification | Letter |
| Similar To |