Device recall
Z-0462-05: Endopath EZ45 No Knife Linear Stapler (NK45G).
FDA device recall · Class II · Ethicon Endo-Surgery
Key facts
| Recall number (Z-number) | Z-0462-05 |
|---|---|
| Recall event | 30516 |
| Product | Endopath EZ45 No Knife Linear Stapler (NK45G). |
| Product code | GDW |
| Recalling firm | Ethicon Endo-Surgery |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Oct 29, 2008 |
| 510(k) numbers | K020779 |
| 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