munevo DRIVE and munevo DRIVE r-net Powered Wheelchair Hands-Free… — Class II medical device recall Z-2856-2026
Ongoing recall by MUNEVO GMBH, reported 2026-08-12, distributed nationwide. A software issue may cause the wheelchair's driving mechanism to fall out of calibration. When this occurs, th
| Recall number | Z-2856-2026 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | MUNEVO GMBH, Munich, Germany |
| Recall initiated | 2026-06-19 |
| Classified | 2026-07-31 |
| Reported by FDA | 2026-08-12 |
| Distributed | Nationwide (US) |
| Countries outside the US | CH, DE, ES, GB, IT |
| Quantity | 19 |
| Reason classes | software |
| UPC / GTIN / UDI-DI | 04260691380010 |
Product
munevo DRIVE and munevo DRIVE r-net Powered Wheelchair Hands-Free Control Application/Smart Glasses Interface/Wheelchair Head Control System
Reason for recall
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2856-2026. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.