Quickie Q7 wheelchair — Class II medical device recall Z-2290-2016
Terminated recall by Sunrise Medical (US) LLC, reported 2016-08-03. There is an observed failure of the backrest bracket which can fatigue over the life time of the product. When
| Recall number | Z-2290-2016 |
|---|---|
| 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 | 2016-07-01 |
| Classified | 2016-07-25 |
| Reported by FDA | 2016-08-03 |
| Terminated | 2017-09-11 |
| Countries outside the US | AE, AR, BH, BR, CL, CN, CR, HK, JP, KR, KW, LB, MX, NL, NZ, SG, SV, UY, ZA |
| Reason classes | device malfunction |
| Model numbers | 000, EIR4 |
Product
Quickie Q7 wheelchair. Model EIR4 Physical Medicine. The Quickie Q7 series of wheelchair's intended use is to provide mobility to persons limited to a sitting position.
Reason for recall
There is an observed failure of the backrest bracket which can fatigue over the life time of the product. When this occurs there is the possibility of the bracket fracturing causing the backrest to detach from the chair frame.
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-2290-2016. 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.