Device recall
Z-0212-04: Ethicon Endo-Surgery Endopath ETS-Flex Articulating Endoscopic Linear Cutter…
FDA device recall · Class II · Ethicon Endo-Surgery
Key facts
| Recall number (Z-number) | Z-0212-04 |
|---|---|
| Recall event | 27763 |
| Product | Ethicon Endo-Surgery Endopath ETS-Flex Articulating Endoscopic Linear Cutter, 35mm Standard, Product #ATB35. |
| Product code | GDW |
| Recalling firm | Ethicon Endo-Surgery |
| Recall class | Class II |
| Status | Terminated |
| Termination date | May 9, 2012 |
| 510(k) numbers | K020779, K961390 |
| FEI number | 1527736 |
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