FDA Device recall Z-1947-2020
Quickie/Zippie powered wheelchair
- FDA Device
- Class II
- terminated
- Published 2020-05-20
On 2020-05-20 the FDA classified a Class II recall of Quickie/Zippie powered wheelchair by Sunrise Medical Us, citing 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.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1947-2020 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2020-02-13 |
| Published | 2020-05-20 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Sunrise Medical Us |
| Distribution | MT |
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
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.
Identifiers
| code_info | Q700M wheelchair S/N Q7MP-083941. UDI:(01)05022408059799. Power Module RNET 120A Expandable (Item No.: 250ER10, Part No…Q700M wheelchair S/N Q7MP-083941. UDI:(01)05022408059799. Power Module RNET 120A Expandable (Item No.: 250ER10, Part No.: 123966). Controller label: D50903.15 CR19100531. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1947-2020%22
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