FDA recall Z-1965-2025

Mobius Mobility LLC · Class II · device

Product

iBOT PMD with software version 01.05.24. Personal Mobility Device.

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.

Key facts

Status
Ongoing
Initiation date
2025-04-24
Report date
2025-06-18
Voluntary/Mandated
Voluntary: Firm initiated
Location
Manchester, NH, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1965-2025