Class II

Medical Device Recall: iBOT PMD with software version 01.05.24. Personal Mobility Device.

Mobius Mobility LLC · April 24, 2025

Reason for Recall

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

Distribution

US Nationwide distribution in the states of CA, CO, FL, GA, IN, NC, NJ, OH, PR, RI, TN, TX & VA.

States Affected

NATIONWIDE

Quantity Affected

442 units

Source: FDA (openFDA Device Enforcement)

Recall number: Z-1965-2025

Status: ongoing

SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.

Mobius Mobility LLC Medical Device Recall: iBOT PMD with software version 01.05.24. Personal Mobility Device. | SafeCheck