FDA Device recall Z-0785-2013
Solara 3G Custom Manual Wheelchair Product Usage: To provide mobility to a person restricted to a sitting position
- FDA Device
- Class II
- terminated
- Published 2013-02-13
On 2013-02-13 the FDA classified a Class II recall of Solara 3G Custom Manual Wheelchair Product Usage: To provide mobility to a person restricted to a sitting position by Invacare, citing the potential exists for the wheel to rotate freely despite engagement of hub brake.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0785-2013 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2012-09-10 |
| Published | 2013-02-13 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Invacare |
| Distribution | US |
Product
Solara 3G Custom Manual Wheelchair Product Usage: To provide mobility to a person restricted to a sitting position.
Reason
The potential exists for the wheel to rotate freely despite engagement of hub brake.
Identifiers
| code_info | Model #3G, Serial numbers: 12GE003750, 12GE003554 and 12HE001766. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0785-2013%22
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