Class II — Permobil Inc
| Recalling firm | Permobil (KunShan) Co., Ltd |
|---|---|
| Registered facility | PERMOBIL (KUNSHAN) CO., LTD (the firm's only registered facility) |
| Classification | Class II |
| Status | Ongoing |
| Reason | This recall has been reported retroactively. The power wheelchair firmware lacks a speed restriction to maintain stability when the seat lift exceeds 50 mm, which may cause the user to fall from the wheelchair or the wheelchair to tip over, |
| Product | Permobil M3 Corpus Power Wheelchair with Heavy Duty Shock REF:120031, Model version 3 |
| Quantity | 140 units |
| Distribution | Worldwide - US Nationwide distribution in the states of AL, AR, AZ, CA, CO, CT, FL, GA, HI, IA, ID, IL, IN, KY, ME, MI, MN, MO, MS, MT, NC, ND, NJ, NV, NY, OH, OK, OR, PA, SC, TN, TX, UT, VA, VT, WA, WI, WV, WY and the country of CAN. |
| Initiated | 2024-02-29 |
| Classified | 2026-07-24 |
| Recall number | Z-2795-2026 |
| 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 — Permobil Inc (Z-2795-2026).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/99315/
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