Device recall
Z-0468-06: BD Perisafe epidural mini-kit: 18 G x 3 1/2 in. Weiss needle. The catheter…
FDA device recall · Class III · Becton Dickinson & Company
Key facts
| Recall number (Z-number) | Z-0468-06 |
|---|---|
| Recall event | 34199 |
| Product | BD Perisafe epidural mini-kit: 18 G x 3 1/2 in. Weiss needle. The catheter connector has four components: body (green), cap (white), washer (white), and gasket (grey). It is used for continuous administration of anesthesia. The product is molded and assembled by Avail, Northeast. It is then supplied… |
| Product code | GCD |
| Recalling firm | Becton Dickinson & Company |
| Recall class | Class III |
| Status | Terminated |
| Termination date | Mar 3, 2008 |
| 510(k) numbers | K850505 |
| FEI number | 2243072 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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