Quickie Q7 Adult Rigid Wheelchair Model EIR4 — Class II medical device recall Z-1020-2015
Terminated recall by Sunrise Medical (US) LLC, reported 2015-02-04, distributed nationwide. There is the potential for the height adjustable handle to dislodge due to failing locking mechanisms on speci
| Recall number | Z-1020-2015 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Sunrise Medical (US) LLC, Fresno, CA, United States |
| Recall initiated | 2014-12-19 |
| Classified | 2015-01-27 |
| Reported by FDA | 2015-02-04 |
| Terminated | 2015-03-10 |
| Distributed | Nationwide (US) |
| Quantity | 6 |
| Serial numbers | R4-024649, R4-024738, R4-024771, R4-025010, R4-025051, R4-025066 |
| Model numbers | EIR4 |
Product
Quickie Q7 Adult Rigid Wheelchair Model EIR4.
Reason for recall
There is the potential for the height adjustable handle to dislodge due to failing locking mechanisms on specific identified chairs.
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-1020-2015. 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.