Quickie/Zippie powered wheelchair — Class II medical device recall Z-1947-2020
Terminated recall by Sunrise Medical (US) LLC, reported 2020-05-20, distributed in MT. Due to programming errors in the Controller, an increase in the set motor parameters can be made by the end us
| Recall number | Z-1947-2020 |
|---|---|
| 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 | 2020-02-13 |
| Classified | 2020-05-11 |
| Reported by FDA | 2020-05-20 |
| Terminated | 2021-04-28 |
| Distributed | MT |
| Quantity | 1 |
| UPC / GTIN / UDI-DI | 05022408059799 |
| Model numbers | 123966, 250ER10 |
Product
Quickie/Zippie powered wheelchair. Q700M wheelchair. A battery operated powered wheelchair, which is controlled by Power Module RNET 120A Expandable (Item No.: 250ER10, Part No.: 123966).
Reason for recall
Due to programming errors in the Controller, an increase in the set motor parameters can be made by the end user beyond tested safe limits.
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-1947-2020. 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.