mo-Vis P002-76Recalls & reported problems
mo-Vis · All-Round Joystick R-net Light · Class 1
Data updated Oct 16, 2026 from official FDA records · Editorial policy
1 open recall names this device. See the recall details and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 0
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 1
Summary
No MAUDE adverse event reports in our data reference this device identifier directly.
1 FDA recall record name this device's identifier, 1 still open.
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.
Recalls naming this device
- Jul 10, 2025Open, Classified
Devices with firmware versions 2.3 and lower may experience timing variations between software tasks, which could result in skipping the necessary neutral check and the wheelchair producing unintended movement upon power-up when the joystick is out of neutral.
Z-2458-2025 · Root cause: Device Design · Recall details · FDA record ↗
Other Components, Wheelchair devices
- mo-Vis P002-77mo-Vis · Components, Wheelchair1 recall0 reports
- mo-Vis IDM-MICRO-Rmo-Vis · Components, Wheelchair1 recall0 reports
- mo-Vis P002-52mo-Vis · Components, Wheelchair1 recall0 reports
- mo-Vis P015-61mo-Vis · Components, Wheelchair1 recall0 reports
- mo-Vis P002-62mo-Vis · Components, Wheelchair1 recall0 reports
- munevo DRIVE V2Munevo Inc. · Components, Wheelchair1 recall0 reports
- mo-Vis IDM-MULTI-Rmo-Vis · Components, Wheelchair1 recall0 reports
- MEDLINE WCAA0139Medline Industries, Inc. · COMPONENTS, WHEELCHAIR2 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026 · each recall links to the FDA recall notice
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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