Device recall
Z-2856-2026: munevo DRIVE and munevo DRIVE r-net Powered Wheelchair Hands-Free Control…
FDA device recall · Class II · MUNEVO GMBH
Key facts
| Recall number (Z-number) | Z-2856-2026 |
|---|---|
| Recall event | 99328 |
| Product | munevo DRIVE and munevo DRIVE r-net Powered Wheelchair Hands-Free Control Application/Smart Glasses Interface/Wheelchair Head Control System |
| Product code | KNN |
| Recalling firm | MUNEVO GMBH |
| Recall class | Class II |
| Status | Open, Classified |
| FEI number | 3021337381 |
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