Device recall
Z-1026-2024: BD BBL Sensi Disc Chloramphenicol- 30 ug, used for semi-quantitative in vitro…
FDA device recall · Class II · Becton Dickinson & Co.
Key facts
| Recall number (Z-number) | Z-1026-2024 |
|---|---|
| Recall event | 93789 |
| Product | BD BBL Sensi Disc Chloramphenicol- 30 ug, used for semi-quantitative in vitro susceptibility testing. Catalog Number 230733and 231274 |
| Product code | JTN |
| Recalling firm | Becton Dickinson & Co. |
| Recall class | Class II |
| Status | Open, Classified |
| FEI number | 1119779 |
At a glance
- None Linked 510(k)s
- 10–99 Products in the same recall event
- 10–99 Recalled products with this product code
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA device recalls (products)
Each recalled device product receives a Z-number. Recall details such as root cause, distribution and firm actions are available in Orca1.
Source: U.S. Food and Drug Administration (FDA), Medical Device Recalls database