[Recalled] 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). — Due to programming errors in the Contro
Regulators flagged this product in an official safety action. Here is what the notice says and what it means for owners.
Recall details
| 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). |
|---|---|
| Brand / manufacturer | Sunrise Medical (US) LLC |
| Category | device |
| Issuing authority | FDA_DEVICE |
| Reference | Z-1947-2020 |
| Country of notice | United States |
| Risk level | Class II |
| Hazard type | recall |
| Notice date | 13 February 2020 |
| EAN / barcode | 05022408059799 |
Why it was recalled
According to the FDA_DEVICE notice, the identified hazard is: 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.
This Class II recall concerns device products distributed in United States and was recorded by FDA_DEVICE. Recalls in this category are published so that owners, retailers, and importers can identify affected units and act quickly.
What to do if you own this product
Check whether your unit is affected and follow the authority's guidance before further use.
Read the full official notice →
Related recalls from Sunrise Medical (US) LLC
This page indexes a public government recall notice for reference. We do not sell or verify this product; always confirm the current status on the authority's official site.
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