Medical DeviceJun 18, 2025
Mobius Mobility iBOT PMD with software version 01.05.24 recall — FDA Z-1965-2025
Software issue that could potentially lead to the device tipping over from Balance Mode.
Class IIFDA: OngoingMobius Mobility LLC
Recall history in this database
Classification mix: Class II: 1.
Understanding this recall history
This page summarizes recall records in which the official source identifies Mobius Mobility LLC as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.