Device recall
Z-0972-2020: Bander Ureteral Diversion Open-End Stent Set, Global Product No. G14822 G14823
FDA device recall · Class II · Cook Inc.
Key facts
| Recall number (Z-number) | Z-0972-2020 |
|---|---|
| Recall event | 82026 |
| Product | Bander Ureteral Diversion Open-End Stent Set, Global Product No. G14822 G14823 |
| Product code | GBL |
| Recalling firm | Cook Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 29, 2020 |
| FEI number | 1820334 |
At a glance
- None Linked 510(k)s
- 10–99 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