Aquila Corporation recalls APK2 Pressure-Sensing Wheelchair Cushions with specific serial numbers due to defective battery packs that can overheat, causing property damage and one possible injury.
Defective battery pack in wheelchair cushions can overheat resulting in property damage and one possible injury.
Aquila Corporation is recalling APK2 Pressure-Sensing Wheelchair Cushions with certain serial numbers because their battery packs can overheat. This risk of property damage and potential injury means affected users should stop using the cushions immediately.
The defective battery pack in these wheelchair cushions can overheat, which may cause property damage and one possible injury. This happens because the battery is not functioning properly and can become too hot under normal use conditions.
People who own or use APK2 Pressure-Sensing Wheelchair Cushions with the listed serial numbers are affected. Those who rely on wheelchairs for mobility are most at risk due to the potential for overheating.
Check the serial number on your APK2 Pressure-Sensing Wheelchair Cushion. The affected units have specific serial numbers listed in the recall notice.
Look for the serial number on the cushion to confirm if it is in the list of affected units.
If your cushion has an affected serial number, stop using it immediately to prevent overheating and potential injury.
The defective battery pack in these cushions can overheat, leading to property damage and one possible injury.
Stop using the cushion immediately and check the serial number to confirm if it is in the list of affected units.
Check the serial number on your cushion against the list of affected serial numbers provided in the recall notice.
We’ve drafted a message you can send Aquila to request your refund or repair — edit it as you like.
Subject: Recall Z-2593-2023 — Aquila Aquila Hello, I own a Aquila that is covered by recall Z-2593-2023 from Aquila. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
