Device recall
Z-2505-2018: Endo GIA 60 mm Extra Thick Black Articulating Reload with Tri-Staple Technology…
FDA device recall · Class II · COVIDIEN MEDTRONIC
Key facts
| Recall number (Z-number) | Z-2505-2018 |
|---|---|
| Recall event | 80423 |
| Product | Endo GIA 60 mm Extra Thick Black Articulating Reload with Tri-Staple Technology, Item Code EGIA60AXT |
| Product code | GDW |
| Recalling firm | COVIDIEN MEDTRONIC |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K111825 |
| FEI number | 1219930 |
At a glance
- 1–9 Linked 510(k)s
- 10–99 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