APK2 Pressure-Sensing Wheelchair Cushions — Class II medical device recall Z-2593-2023
Ongoing recall by Aquila Corporation, reported 2023-09-27, distributed nationwide. Defective battery pack in wheelchair cushions can overheat resulting in property damage and one possible injur
| Recall number | Z-2593-2023 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Aquila Corporation, Holmen, WI, United States |
| Recall initiated | 2023-07-06 |
| Classified | 2023-09-18 |
| Reported by FDA | 2023-09-27 |
| Distributed | Nationwide (US) |
| Countries outside the US | AU, CA, GB, RO, SE |
| Quantity | 117 units |
| Reason classes | device malfunction |
| Serial numbers | 3213, 3878, 4661, 4754, 5270, 5527, 5532, 5754, 5766, 5771, 5811, 5830, 5877, 5908, 6177, 6181, 6326, 6337, 6596, 6808, 6833, 6837, 6865, 6879, 6901 and 68 more |
Product
APK2 Pressure-Sensing Wheelchair Cushions
Reason for recall
Defective battery pack in wheelchair cushions can overheat resulting in property damage and one possible injury.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2593-2023. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.