Holmen, WI, United States
Aquila Corporation recalls
1 recall recorded since 2018, most recently on 6 July 2023. 1 is listed as ongoing. Status and classification are as published by the FDA.
Recalls1
Ongoing (FDA)1
Terminated or completed0
Class I (FDA)0
Ongoing Class II Medical devices
- Recall started
- 6 July 2023
- Reason
- Defective battery pack in wheelchair cushions can overheat resulting in property damage and one possible injury.
- Distribution
- Worldwide distribution: US (nationwide) and OUS (foreign) countries of: Canada, Sweden, Romania, Australia, UK
- Initiated
- Voluntary: Firm initiated
- Recall numbers
- Z-2593-2023, Z-2594-2023
- APK2 Pressure-Sensing Wheelchair Cushions
- SofTech Pressure-Sensing Wheelchair Cushions
A terminated FDA recall means the FDA has determined that all reasonable efforts to remove or correct the product have been made. What statuses mean.