FDAApril 24, 2025device
iBOT PMD with software version 01.05.24. Personal Mobility Device.
Official recall recorded by the U.S. Food & Drug Administration.
The hazard
Software issue that could potentially lead to the device tipping over from Balance Mode.
What to do
FDA enforcement status: Ongoing
Brands named
mobius mobilitymobius
UPCs
00857584008010
Recall history
Other federal recalls tied to the same brand — a factual pattern, straight from the source data.
- CPSCAdult Portable Bed Rails Recalled Due to Risk of Serious Injury or Death from Entrapment and Asphyxiation; Violate Mandatory Standard for Adult Portable Bed Rails; Imported by Hepo Care Medical Equipment Online2026-04-30
- FDADetachable 10in Pend FRU-1 Pend component for the AIRO Computed Tomography (CT) X-ray System.2025-12-04
- FDADetachable 10in Pendant Upgrade component for the AIRO Computed Tomography (CT) X-ray System.2025-12-04
- CPSCLEACHOI Adult Portable Bed Rails Recalled Due to Risk of Serious Injury or Death from Entrapment and Asphyxiation; Violates Mandatory Standard for Adult Portable Bed Rails; Sold on Amazon by LEACHOI2025-10-23
- FDAMax Mobility/Permobil Smart Drive MX2+ SpeedControl Dial Ref: MX2-3DCMC use in conjunction with the SmartDrive MX2+ Wheelchair Power Assist component.2025-08-12
- FDAMax Mobility/Permobil Smart Drive MX2+ SpeedControl Dial Ref: MX2-3DC use in conjunction with the SmartDrive MX2+ Wheelchair Power Assist component.2025-08-12
- FDAMax Mobility/Permobil Smart Drive MX2+ SpeedControl Dial Ref: MX2-3DCK use in conjunction with the SmartDrive MX2+ Wheelchair Power Assist component.2025-08-12
- FDAMax Mobility/Permobil Smart Drive MX2+ SpeedControl Dial Ref: MX2-3DC use in conjunction with the SmartDrive MX2+ Wheelchair Power Assist component.2024-12-20
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