Device recall
Z-0700-2024: VADER pedicle system, torque wrench, Catalog Number 42-702
FDA device recall · Class II · Icotec Ag
Key facts
| Recall number (Z-number) | Z-0700-2024 |
|---|---|
| Recall event | 93577 |
| Product | VADER pedicle system, torque wrench, Catalog Number 42-702 |
| Product code | PML |
| Recalling firm | Icotec Ag |
| Recall class | Class II |
| Status | Open, Classified |
| 510(k) numbers | K222789 |
| FEI number | 3006493760 |
At a glance
- 1–9 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