CLASS II ONGOING Device recall · Reported 27 Sep 2023 · FDA Enforcement Report
APK2 Pressure-Sensing Wheelchair Cushions recalled by Aquila
Aquila is recalling APK2 Pressure-Sensing Wheelchair Cushions, distributed nationwide in the US. The recall was initiated on 6 Jul 2023 and the FDA has classified it as Class II.
Check your package
Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.
Recall details
- Recall number
- Z-2593-2023
- FDA event ID
- 92790
- Recalling firm
- Aquila, Holmen, WI
- Classification
- Class II
- Status
- Ongoing
- Recall initiated
- 6 Jul 2023
- FDA classified
- 18 Sep 2023
- Reported
- 27 Sep 2023
- Type
- Voluntary: Firm initiated
- Customers notified by
- Letter
- Reason category
- Device Malfunction
- Device type
- Wheelchairs, Beds & Lifts
Timeline
| 6 Jul 2023 | Recall initiated by company | |
| 18 Sep 2023 | Classified by FDA | +74 days |
| 27 Sep 2023 | Published in enforcement report | +9 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Defective battery pack in wheelchair cushions can overheat resulting in property damage and one possible injury.
Device recalls are issued when a component, software or design fault could cause the device to fail or give wrong readings. Many are corrections applied in the field rather than physical returns.
Product as listed by the FDA
APK2 Pressure-Sensing Wheelchair Cushions
Where it was distributed
Worldwide distribution: US (nationwide) and OUS (foreign) countries of: Canada, Sweden, Romania, Australia, UK
Questions about this recall
Why was it recalled?
Defective battery pack in wheelchair cushions can overheat resulting in property damage and one possible injury.
Which lots are affected?
Serial Numbers: 3213, 3878, 4661, 4754, 5270, 5527, 5532, 5754, 5766, 5771, 5771, 5811, 5830, 5877, 5908, 6177, 6181, 6326, 6337, 6596, 6808, 6833, 6837, 6865, 6879, 6901, 6903, 6949, 6967, 6983, 6988, 6988, 6991, 6992, 6993, 6993, 6998, 6998, 6999, 6999, 7003, 7012, 7012, 7013, 7013, 7013, 7014, 7015, 7015, 7019, 7019, 7024, 7027, 7028, 7029, 7034, 7035, 7036, 7036, 7037, 7037, 7056, 7056, 7057, 7063, 7064, 7078, 7087, 7088, 7088, 7090, 7090, 7504, 7515, 7619, 7673, 7696, 7725, 7764, 7782, 7838, 7867, 7869, 7869, 7877, 7878, 7878, 7879, 7880, 7884, 7888, 7889, 7890, 7890, 7891, 7901, 7901, 7902, 7903, 7903, 7937, 7945, 7946, 7947, 7948, 7953, 7954, 7955, 7955, 7975, 7975, 7976, 7977, 7977, 7991, 7991, 7992
Where was it sold?
Worldwide distribution: US (nationwide) and OUS (foreign) countries of: Canada, Sweden, Romania, Australia, UK
What should I do if I have it?
Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.
What does Class II mean?
Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.
Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
Other products in this recall event
1 other product · FDA event 92790| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| CLASS II | SofTech Pressure-Sensing Wheelchair Cushions recalled by Aquila | Aquila | Device Malfunction | Nationwide |
More recalls from Aquila
All 2| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Device | CLASS II | SofTech Pressure-Sensing Wheelchair Cushions recalled by Aquila | Aquila | Device Malfunction | Nationwide |
Other Wheelchairs, Beds & Lifts recalls
All 172| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Device | CLASS II | Quantum Rehab Quantum 4Front 2HD recalled by Pride Mobility Products | Pride Mobility Products | Device Malfunction | Nationwide |
| Device | CLASS II | Quantum Rehab Q6 Edge 2.0 (ilevel) recalled by Pride Mobility Products | Pride Mobility Products | Device Malfunction | Nationwide |
| Device | CLASS II | Quantum Rehab Q6 Edge recalled by Pride Mobility Products | Pride Mobility Products | Device Malfunction | Nationwide |
| Device | CLASS II | Quantum rehab Q6 Edge recalled by Pride Mobility Products | Pride Mobility Products | Device Malfunction | Nationwide |
| Device | CLASS II | Quantum Rehab Q6 Edge recalled by Pride Mobility Products | Pride Mobility Products | Device Malfunction | Nationwide |