Class II — Permobil, Ab
| Recalling firm | Permobil (KunShan) Co., Ltd |
|---|---|
| Registered facility | PERMOBIL (KUNSHAN) CO., LTD (the firm's only registered facility) |
| Classification | Class II |
| Status | Terminated |
| Reason | This correction decision has been made because of a potential failure of one or both backrest bars providing back support. If one or both back support telescoping bars fail the user could fall back leading to a potential injury. |
| Product | Permobil powered wheelchairs, Model Numbers: (a) M300 PS, (b) C300 PS, (c) C350 PS, (d) C500 PS, (e) C400 PS Product Usage: The devices identified are intended to provide outdoor and indoor mobility to persons limited to a seated position that can operate a powered wheelchair. |
| Quantity | 3134 units |
| Distribution | Worldwide Distribution - US Nationwide |
| Initiated | 2018-08-15 |
| Classified | 2018-09-14 |
| Terminated | 2021-05-03 |
| Recall number | Z-3178-2018 |
| 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, Ab (Z-3178-2018).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/80686/
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