DeviceSignal · Recall classified
MUNEVO GMBH
FDA classified a device recall on 2026-07-31 · Class II · Z-2856-2026
EventRecall classified
Effective2026-07-31
ClassificationClass II
On 2026-07-31 the FDA classified a device recall from MUNEVO GMBH as Class II. Product: munevo DRIVE and munevo DRIVE r-net Powered Wheelchair Hands-Free Control…. Recall Z-2856-2026. The firm initiated it on 2026-06-19. This reports the classification FDA published on that date.
Reported facts
- Recall number
- Z-2856-2026
- Classification
- Class II
- Classified on
- 2026-07-31
- Initiated on
- 2026-06-19
- Firm
- MUNEVO GMBH
- 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
Every field above is as fda_device_enforcement published it. Nothing on this page is our interpretation.
Provenance
- Source
- fda_device_enforcement
- Source record
Z-2856-2026- Snapshot hash
ab5ada73bf212eb52a548aab0968a0fcee42807c61b0350e60e24bb6e2beed72- Source URL
- https://download.open.fda.gov/device/enforcement/device-enforcement-0001-of-0001.json.zip
- Observed
- 2026-09-08T16:22:09.483Z
- Transform
fda_device_enforcement_to_recall v1- Event rule
fda_device_recall_classified v1- Event key
db803d22b6fb0ed525dcef6e7e663b368fb46425b54b5383bdb2bda3ee9f4f22- Signal type
device_recall.classified
Source terms that apply
- This is not a public alerting service and must not be used to notify patients or the public
- We do not report whether a recall is still open; FDA does not maintain that after classification
- Nothing here is a medical or clinical decision aid
- Not affiliated with, endorsed by, or certified by the FDA
Data provided by the U.S. Food and Drug Administration (https://open.fda.gov)