Class II — Sunrise Medical (US) LLC
| Recalling firm | Sunrise Medical International Inc. |
|---|---|
| Registered facility | SUNRISE MEDICAL INTERNATIONAL INC. (the firm's only registered facility) |
| Classification | Class II |
| Status | Terminated |
| Reason | 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. |
| 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). |
| Quantity | 1 |
| Distribution | Distributed to US Consignee in MT. |
| Initiated | 2020-02-13 |
| Classified | 2020-05-11 |
| Terminated | 2021-04-28 |
| Recall number | Z-1947-2020 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — Sunrise Medical (US) LLC (Z-1947-2020).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/85431/
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