APK2 Wheelchair Cushion Battery Pack Defect Can Cause Overheating
Aquila Corporation recalls 117 APK2 wheelchair cushions with defective battery packs that can overheat. The risk could result in property damage and injury.
What this means for you
Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.
Our severity reasoning: This is an FDA Class II device recall involving a known defect (battery overheating) that poses risk of property damage and possible injury, though no confirmed injuries have yet been reported. This qualifies as a risk-of-harm product where injury has not been reported, per the severity rubric.
Plain-English summary
Aquila Corporation is recalling 117 units of the APK2 Pressure-Sensing Wheelchair Cushion because the product's battery pack can overheat. This defect poses a risk of property damage and injury.
The recalled products were distributed worldwide, including to consumers in the United States, Canada, Sweden, Romania, Australia, and the United Kingdom. Consumers can verify whether their cushion is affected by checking its serial number against the list provided in the recall notice.
Further details about the recall and next steps are available through Aquila Corporation or the FDA.
The recalled product
- Product
- APK2 Pressure-Sensing Wheelchair Cushions
- Manufacturer
- Aquila Corporation
- Category
- Medical Device — Mobility
- Hazard
- battery-defect
- overheating
- property-damage
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (20)
- Serial Numbers: 3213
- 3878
- 4661
- 4754
- 5270
- 5527
- 5532
- 5754
- 5766
- 5771
- 5811
- 5830
- 5877
- 5908
- 6177
- 6181
- 6326
- 6337
- 6596
- 6808
Distribution
Distributed nationwide across the United States.
Related recalls
Same category
- HighAzurion X-ray System Deaeration Hose May Degrade and Cause Oil Leakage
FDA (Devices) · 2026-05-27
- SevereMedtronic DLP Retrograde Cannula recalled for sterile barrier breach risk
FDA (Devices) · 2026-05-27
- SevereMedtronic DLP Retrograde Cannula Recalls for Sterile Barrier Breach Risk
FDA (Devices) · 2026-05-27
- HighSwan-Ganz Jr Catheter models recalled due to lumen hub leakage
FDA (Devices) · 2026-05-27
- HighMedtronic DLP Retrograde Cannula Cardiopulmonary Bypass Catheter Recall
FDA (Devices) · 2026-05-27