Electric Wheelchair bases: a) C300 b) C350 c) C400 d) C500 — Class II medical device recall Z-0006-2018
Terminated recall by Permobil, Ab, reported 2017-10-11, distributed nationwide. There is a potential failure of the top plate assembly, which is the component that connects the seating syste
| Recall number | Z-0006-2018 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Permobil, Ab, Timra, N/A, Sweden |
| Recall initiated | 2017-09-01 |
| Classified | 2017-10-03 |
| Reported by FDA | 2017-10-11 |
| Terminated | 2021-05-04 |
| Distributed | Nationwide (US) |
| Countries outside the US | AE, AU, CA, DE, DK, FI, FR, IL, NO, SE |
| Quantity | 146 units |
Product
Electric Wheelchair bases: a) C300 b) C350 c) C400 d) C500
Reason for recall
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0006-2018. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.