Device recall
Z-0671-2024: SPRYSTEP VECTOR, Custom made device dynamic ankle-foot orthosis (AFO)…
FDA device recall · Class II · Townsend Design
Key facts
| Recall number (Z-number) | Z-0671-2024 |
|---|---|
| Recall event | 93299 |
| Product | SPRYSTEP VECTOR, Custom made device dynamic ankle-foot orthosis (AFO) , Reference numbers: 17V1030, 17V2030, 17V1031, 17V2031, 17V1032, 17V2032, 17V1033, 17V2033, 17V1035, 17V2035, 17V1036, 17V2036, 17V1037, 17V2037 |
| Product code | IQI |
| Recalling firm | Townsend Design |
| Recall class | Class II |
| Status | Completed |
| FEI number | 1000523125 |
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