Device recall
Z-0958-04: Auto Suture TA 30 Reloadable Staplers, Single Patient Use Ref TA30V3S, V3…
FDA device recall · Class II · United States Surgical
Key facts
| Recall number (Z-number) | Z-0958-04 |
|---|---|
| Recall event | 28998 |
| Product | Auto Suture TA 30 Reloadable Staplers, Single Patient Use Ref TA30V3S, V3 (2.5mm) DST Series |
| 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