PlainRecalls
FDA Devices Moderate Class II Ongoing

iBOT PMD with software version 01.05.24. Personal Mobility Device.

Reported: June 18, 2025 Initiated: April 24, 2025 #Z-1965-2025

Product Description

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.

Details

Recalling Firm
Mobius Mobility LLC
Units Affected
442 units
Distribution
US Nationwide distribution in the states of CA, CO, FL, GA, IN, NC, NJ, OH, PR, RI, TN, TX & VA.
Location
Manchester, NH

Frequently Asked Questions

What product was recalled?
iBOT PMD with software version 01.05.24. Personal Mobility Device.. Recalled by Mobius Mobility LLC. Units affected: 442 units.
Why was this product recalled?
Software issue that could potentially lead to the device tipping over from Balance Mode.
Which agency issued this recall?
This recall was issued by the FDA Devices on June 18, 2025. Severity: Moderate. Recall number: Z-1965-2025.