Device recall
Z-1501-06: Neoligaments Staple Impactor, 8 mm Staple Impactor: 202-3010
FDA device recall · Class II · Xiros Plc
Key facts
| Recall number (Z-number) | Z-1501-06 |
|---|---|
| Recall event | 35828 |
| Product | Neoligaments Staple Impactor, 8 mm Staple Impactor: 202-3010 |
| Product code | HXJ |
| Recalling firm | Xiros Plc |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Sep 14, 2012 |
| FEI number | 3013299874 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 1–9 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