Device recall
Z-2617-2016: Kumpe Access Catheter Cathether, Ureteral, General & Plastic Surgery Used in…
FDA device recall · Class II · Cook Inc.
Key facts
| Recall number (Z-number) | Z-2617-2016 |
|---|---|
| Recall event | 74010 |
| Product | Kumpe Access Catheter Cathether, Ureteral, General & Plastic Surgery Used in combination with a HiWire, Bentson, or other flexible-tipped wire guide to gain difficult ureteral access beyond a redundant or tortuous ureteral segment |
| Product code | GBL |
| Recalling firm | Cook Inc. |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Aug 4, 2017 |
| 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