Device recall
Z-0960-04: Auto SutureTA 30 Reloadable Stapler,Single Patient Use, 4.8mm DST Series Ref…
FDA device recall · Class II · United States Surgical
Key facts
| Recall number (Z-number) | Z-0960-04 |
|---|---|
| Recall event | 28998 |
| Product | Auto SutureTA 30 Reloadable Stapler,Single Patient Use, 4.8mm DST Series Ref: TA30348S |
| Product code | GDW |
| Recalling firm | United States Surgical |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Nov 15, 2006 |
| 510(k) numbers | K013860 |
| FEI number | 1219930 |
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