[Recalled] 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. — There is an observed failure of the backrest bracket w
The product on this page is subject to an official recall. We summarise the regulator's findings and the recommended action.
Recall details
| 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. |
|---|---|
| Brand / manufacturer | Sunrise Medical (US) LLC |
| Category | device |
| Issuing authority | FDA_DEVICE |
| Reference | Z-2290-2016 |
| Country of notice | United States |
| Risk level | Class II |
| Hazard type | recall |
| Notice date | 01 July 2016 |
Why it was recalled
According to the FDA_DEVICE notice, the identified hazard is: 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.
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.