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 | There is a potential failure of the top plate assembly, which is the component that connects the seating system of the wheelchair to the base. |
| Product | Electric Wheelchairs: a) C300 CORPUS II b) C350 CORPUS II c) C400 CORPUS II d) C400 CORPUS II LR e) C500 CORPUS II f) C500 CORPUS II LR |
| Quantity | 5539 units |
| Distribution | Nationwide and Australia, Benelux, Canada, Denmark, Finland, France, Germany, Israel, Norway, Sweden, and UAE |
| Initiated | 2017-09-01 |
| Classified | 2017-10-03 |
| Terminated | 2021-05-04 |
| Recall number | Z-0005-2018 |
| 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-0005-2018).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/78079/
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