Class II — Mobius Mobility LLC
| Recalling firm | Mobius Mobility LLC |
|---|---|
| Registered facility | MOBIUS MOBILITY LLC (the firm's only registered facility) |
| Classification | Class II |
| Status | Ongoing |
| Reason | Software issue that could potentially lead to the device tipping over from Balance Mode. |
| Product | iBOT PMD with software version 01.05.24. Personal Mobility Device. |
| Quantity | 442 units |
| Distribution | US Nationwide distribution in the states of CA, CO, FL, GA, IN, NC, NJ, OH, PR, RI, TN, TX & VA. |
| Initiated | 2025-04-24 |
| Classified | 2025-06-12 |
| Recall number | Z-1965-2025 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — Mobius Mobility LLC (Z-1965-2025).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/96834/
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