Class II — MUNEVO GMBH
| Recalling firm | Munevo GmBH |
|---|---|
| Registered facility | MUNEVO GMBH (the firm's only registered facility) |
| Classification | Class II |
| Status | Ongoing |
| Reason | A software issue may cause the wheelchair's driving mechanism to fall out of calibration. When this occurs, the device may experience unexpected steering drift or imprecise control while driving the wheelchair. The wheelchair may veer from its intended path, which may cause in low-speed collision, tipping, or injuries to user or bystanders. |
| Product | munevo DRIVE and munevo DRIVE r-net Powered Wheelchair Hands-Free Control Application/Smart Glasses Interface/Wheelchair Head Control System |
| Quantity | 19 |
| Distribution | Worldwide - US Nationwide distribution in the states of California, Florida, North Carolina, Texas, Utah, and Washington. The countries of United Kingdom, Spain, Italy, Germany, and Switzerland. |
| Initiated | 2026-06-19 |
| Classified | 2026-07-31 |
| Recall number | Z-2856-2026 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — MUNEVO GMBH (Z-2856-2026).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/99328/
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