Solara 3G Custom Manual Wheelchair Product Usage: To provide mobility… — Class II medical device recall Z-0785-2013
Terminated recall by Invacare Corporation, reported 2013-02-13, distributed nationwide. The potential exists for the wheel to rotate freely despite engagement of hub brake.
| Recall number | Z-0785-2013 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Invacare Corporation, Elyria, OH, United States |
| Recall initiated | 2012-09-10 |
| Classified | 2013-02-04 |
| Reported by FDA | 2013-02-13 |
| Terminated | 2014-05-13 |
| Distributed | Nationwide (US) |
| Quantity | 3 units |
| Serial numbers | 12GE003554, 12GE003750, 12HE001766 |
Product
Solara 3G Custom Manual Wheelchair Product Usage: To provide mobility to a person restricted to a sitting position.
Reason for recall
The potential exists for the wheel to rotate freely despite engagement of hub brake.
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-0785-2013. 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.