Mobius Mobility LLC: Device Recall
Recall #Z-1965-2025 · 04/24/2025
Class II: Risk
Recall Details
- Recall Number
- Z-1965-2025
- Classification
- Class II
- Product Type
- Device
- Recalling Firm
- Mobius Mobility LLC
- Status
- Ongoing
- Date Initiated
- 04/24/2025
- Location
- Manchester, NH, United States
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 442 units
Reason for Recall
Software issue that could potentially lead to the device tipping over from Balance Mode.
Product Description
iBOT PMD with software version 01.05.24. Personal Mobility Device.
Distribution Pattern
US Nationwide distribution in the states of CA, CO, FL, GA, IN, NC, NJ, OH, PR, RI, TN, TX & VA.
Data from FDA openFDA enforcement reports. This site is not affiliated with or endorsed by the FDA. Recall information may be updated by the FDA at any time.