Mobius Mobility LLC: Medical Device Recall in 2025 - (Recall #: Z-1965-2025)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2025.

Data Source: FDA.

Product Description:

iBOT PMD with software version 01.05.24. Personal Mobility Device.

Product Classification:

Class II

Date Initiated: April 24, 2025

Date Posted: June 18, 2025

Recall Number: Z-1965-2025

Event ID: 96834

Reason for Recall:

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

Status: Ongoing

Product Quantity: 442 units

Code Information:

Software Version 01.05.24; UDI (01) 00857584008010 (21) 0001108, (01) 00857584008010 (21) 0001110, (01) 00857584008010 (21) 0001121, (01) 00857584008010 (21) 0001123, (01) 00857584008010 (21) 0001128, (01) 00857584008010 (21) 0001136, (01) 00857584008010 (21) 0001137, (01) 00857584008010 (21) 0001422, (01) 00857584008010 (21) 0001438, (01) 00857584008010 (21) 0001496, (01) 00857584008010 (21) 0001505, (01) 00857584008010 (21) 0001508, (01) 00857584008010 (21) 0001516, (01) 00857584008010 (21) 0001517, (01) 00857584008010 (21) 0001519; Serial No. 0001108, 0001422, 0001438, 0001496, 0001505, 0001508, 0001516, 0001517, 0001519, 0001110, 0001121, 0001123, 0001128, 0001136, 0001137.

Distribution Pattern:

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

Voluntary or Mandated:

Voluntary: Firm initiated