Munevo Gmbh: Components, Wheelchair
Recall Summary MUNEVO GMBH is recalling munevo DRIVE and munevo DRIVE r-net powered wheelchairs with hands-free control systems due to a software problem that can cause the wheelchair to lose steering calibration. When this happens, the wheelchair may steer unexpectedly or not respond precisely to commands, potentially causing it to veer off course and result in collisions, tipping, or injury. The affected wheelchairs were distributed nationwide in the U.S. and in the United Kingdom, Spain, Italy, Germany, and Switzerland.
- Recalling firm
- MUNEVO GMBH
- Product
- munevo DRIVE and munevo DRIVE r-net Powered Wheelchair Hands-Free Control Application/Smart Glasses Interface/Wheelchair Head Control System
- 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.
- Classification
- Class I
- Category
- medical device recall
- Country
- United States
- Agency
- FDA-DEVICES
- Recall date
- 2026-06-19
- Status
- Open, Classified
- Areas affected
- AL, AK, AZ, AR, CA, CO, CT, DE, FL, GA, HI, ID, ...
- 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.
Official recall notice from FDA-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/c73762a4-9dde-4c4c-bd9c-52a1a1c5c242