Device recall
Z-1271-2019: Endoscopic Curved Intraluminal Stapler, 21 mm diameter, Model ECS21A The Ethicon…
FDA device recall · Class I · Ethicon Endo-Surgery Inc
Key facts
| Recall number (Z-number) | Z-1271-2019 |
|---|---|
| Recall event | 82539 |
| Product | Endoscopic Curved Intraluminal Stapler, 21 mm diameter, Model ECS21A The Ethicon Endo-Surgery Intraluminal Staplers (ILS) are anastomotic staplers available in four sizes to permit proper matching of instrument to diameter of the lumen. The instrument permits tissue attachment to the anvil shaft in… |
| Product code | GDW |
| Recalling firm | Ethicon Endo-Surgery Inc |
| Recall class | Class I |
| Status | Completed |
| 510(k) numbers | K940967, K983536 |
| 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