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Mobius Mobility LLC recalls iBOT PMD with software version 01.05.24. Personal Mobility Device.
Recalled June 18, 2025 · FDA recall Z-1965-2025 · Mobius Mobility
Hazard
Software issue that could potentially lead to the device tipping over from Balance Mode. · FDA Class II
Units
442 units
Sold at
US Nationwide distribution in the states of CA, CO, FL, GA, IN, NC, NJ, OH, PR, RI, TN, TX & VA.
Description
Software issue that could potentially lead to the device tipping over from Balance Mode.
Product
iBOT PMD with software version 01.05.24. Personal Mobility Device.
Manufacturer(s)
Mobius Mobility LLC
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →