FDA Device recall Z-1965-2025
iBOT PMD with software version 01.05.24
- FDA Device
- Class II
- ongoing
- Published 2025-06-18
On 2025-06-18 the FDA classified a Class II recall of iBOT PMD with software version 01.05.24 by Mobius Mobility, citing software issue that could potentially lead to the device tipping over from Balance Mode.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1965-2025 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2025-04-24 |
| Published | 2025-06-18 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | Mobius Mobility |
| Distribution | US |
Product
iBOT PMD with software version 01.05.24. Personal Mobility Device.
Reason
Software issue that could potentially lead to the device tipping over from Balance Mode.
Identifiers
| code_info | Software Version 01.05.24; UDI (01) 00857584008010 (21) 0001108, (01) 00857584008010 (21) 0001110, (01) 00857584008010…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. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:57 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1965-2025%22
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