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 is being reported retroactively. Power Platform firmware is missing specific drive inhibit logic. This issue may allow the chair to drive under restricted conditions, and may create an unstable condition in certain circumstances. |
| Product | M5 Corpus Power Wheelchair REF,120032 |
| Quantity | 715 wheelchairs |
| 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 CANADA. |
| Initiated | 2025-06-19 |
| Classified | 2026-07-24 |
| Recall number | Z-2805-2026 |
| 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-2805-2026).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/99267/
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