Device recall
Z-0821-2016: Covidien Endo GIA Ultra Universal 12 mm XL Stapler Handle Ref: EGIAUXL Product…
FDA device recall · Class II · Medtronic
Key facts
| Recall number (Z-number) | Z-0821-2016 |
|---|---|
| Recall event | 72749 |
| Product | Covidien Endo GIA Ultra Universal 12 mm XL Stapler Handle Ref: EGIAUXL Product Usage: The Endo GIA Ultra Universal Short, Endo GIA Ultra Universal and Endo GIA Ultra Universal XL staplers have applications in abdominal, gynecologic, pediatric and thoracic surgery for resection, transection and… |
| Product code | GDW |
| Recalling firm | Medtronic |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jul 18, 2019 |
| 510(k) numbers | K111825 |
| FEI number | 1219930 |
At a glance
- 1–9 Linked 510(k)s
- 1–9 Products in the same recall event
- 100–999 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