Mobius Mobility LLC recalls iBOT PMD with software version 01.05.24. Personal Mobility Device.
- Recall date
- April 24, 2025
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- Z-1965-2025
- FDA classification
- Class II
- Brand / firm
- Mobius Mobility LLC
- Sold / distributed
- US Nationwide distribution in the states of CA, CO, FL, GA, IN, NC, NJ, OH, PR, RI, TN, TX & VA.
Why it was recalled
Software issue that could potentially lead to the device tipping over from Balance Mode.
Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.
What was recalled
iBOT PMD with software version 01.05.24. Personal Mobility Device.
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