Device recall
Z-0200-2020: ECHELON FLEX ENDOPATH 60mm Stapler - 340mm shaft, Product Code EC60A
FDA device recall · Class I · Ethicon Endo-Surgery Inc
Key facts
| Recall number (Z-number) | Z-0200-2020 |
|---|---|
| Recall event | 83897 |
| Product | ECHELON FLEX ENDOPATH 60mm Stapler - 340mm shaft, Product Code EC60A |
| Product code | GDW |
| Recalling firm | Ethicon Endo-Surgery Inc |
| Recall class | Class I |
| Status | Terminated |
| Termination date | Jun 3, 2021 |
| 510(k) numbers | K081146 |
| FEI number | 1527736 |
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