FDA Device recall Z-1020-2015
Quickie Q7 Adult Rigid Wheelchair Model EIR4
- FDA Device
- Class II
- terminated
- Published 2015-02-04
On 2015-02-04 the FDA classified a Class II recall of Quickie Q7 Adult Rigid Wheelchair Model EIR4 by Sunrise Medical Us, citing there is the potential for the height adjustable handle to dislodge due to failing locking mechanisms on specific identified chairs.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1020-2015 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2014-12-19 |
| Published | 2015-02-04 |
| Last updated | 2026-09-13 11:53 UTC |
| Company | Sunrise Medical Us |
| Distribution | US |
Product
Quickie Q7 Adult Rigid Wheelchair Model EIR4.
Reason
There is the potential for the height adjustable handle to dislodge due to failing locking mechanisms on specific identified chairs.
Identifiers
| code_info | Serial numbers: R4-025066, R4-025051, R4-025010, R4-024771, R4-024738, R4-024649. |
|---|
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-1020-2015%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.