Device recall
Z-0968-2007: Medtronic U-CLIP Anastomotic Device Removal Tool, model REM1860FW. The U-Clip…
FDA device recall · Class II · Medtronic Cardiac Surgery Technologies
Key facts
| Recall number (Z-number) | Z-0968-2007 |
|---|---|
| Recall event | 37300 |
| Product | Medtronic U-CLIP Anastomotic Device Removal Tool, model REM1860FW. The U-Clip Anastomotic Device Removal Tool is designed to remove U-Clip Anastomotic Devices. |
| Product code | FZP |
| Recalling firm | Medtronic Cardiac Surgery Technologies |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Feb 24, 2008 |
| 510(k) numbers | K031623 |
| FEI number | 3003368396 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 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