Device recall
Z-0072-2022: ARCH Leg Positioning System
FDA device recall · Class II · Innovative Orthopedic Technologies, LLC
Key facts
| Recall number (Z-number) | Z-0072-2022 |
|---|---|
| Recall event | 88636 |
| Product | ARCH Leg Positioning System |
| Product code | BWN |
| Recalling firm | Innovative Orthopedic Technologies, LLC |
| Recall class | Class II |
| Status | Terminated |
| Termination date | Jan 29, 2024 |
| FEI number | 3006119126 |
At a glance
- None Linked 510(k)s
- 1–9 Products in the same recall event
- 10–99 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