Device recall
Z-0908-2018: Endo GIA" Radial Reload with Tri-Staple" Technology The Endo GIA radial reloads…
FDA device recall · Class II · Covidien LLC
Key facts
| Recall number (Z-number) | Z-0908-2018 |
|---|---|
| Recall event | 79166 |
| Product | Endo GIA" Radial Reload with Tri-Staple" Technology The Endo GIA radial reloads with Tri-Staple Technology have application in open or minimally invasive general abdominal, gynecologic and thoracic surgery for resection and transection of tissue and creation of anastomosis, as well as application… |
| Product code | GDW |
| Recalling firm | Covidien LLC |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Dec 19, 2018 |
| 510(k) numbers | K132493 |
| 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