Mobius Mobility LLC recalls iBOT PMD with software version 01.05.24. Personal Mobility Device.

Software issue that could potentially lead to the device tipping over from Balance Mode.

Consignees were initially contacted via telephone on 4/24/25 to notify them of this software issue. An URGENT MEDICAL DEVICE CORRECTION NOTICE dated 5/5/25 was emailed to consignees to notify them of the recall and instructing them that the firm is developing a software correction. Once Mobius Mobility has obtained a correction they will reach out to consignees to schedule a time to update affected devices. Consignees with any questions can email service @mobiusmobility.com or call 833-346-4268x2.

• FDA enforcement recordOfficial FDA database entry for Z-1965-2025
• FDA 510(k) clearance · K243442The device's official FDA premarket clearance record
• FDA device classification · IMKOfficial FDA classification for this device type
• CFR regulation · 21 CFR 890.3890The federal regulation governing this device
• FDA recall announcementSearch FDA.gov for the official press announcement
• Find Mobius Mobility LLCSearch for the manufacturer's official notice
• News coverageRecent reporting on this recall and manufacturer
• openFDA data recordThe raw JSON record this page is built from

Source: U.S. FDA openFDA device enforcement reports. This summary is informational and may lag or differ from the official record. Always verify against the FDA before acting.