Drugs & medicalClass II

Mobius Mobility LLC recalls iBOT PMD with software version 01.05.24. Personal Mobility Device.

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

Read the official notice →
Date
2025-06-18
Country
United States
Brand
Mobius Mobility LLC
Product
iBOT PMD with software version 01.05.24. Personal Mobility Device.
Classification
Class II
Units
US Nationwide distribution in the states of CA, CO, FL, GA, IN, NC, NJ, OH,…
Category
Drugs & medical
Source
FDA · Device

Copied automatically from the US Food and Drug Administration. Details may be shortened or out of date; the official notice is the authoritative source. Disclaimer

What to do

  1. Check the product name, strength and lot number against the official notice.
  2. Do not stop a prescribed medicine without talking to your doctor or pharmacist first.
  3. Ask the pharmacy or supplier about a replacement or refund.

General guidance from Recall Atlas. The official notice from the US Food and Drug Administration has the exact models, batch codes and remedy, and it takes priority.

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