---
title: "APK2 Pressure-Sensing Wheelchair Cushions — FDA record Z-2593-2023 | Is It on Recall"
description: "Defective battery pack in wheelchair cushions can overheat resulting in property damage and one possible injury."
url: https://isitonrecall.com/recall/fda-device-z-2593-2023-apk2-pressure-sensing-wheelchair-cushions/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

[Recall archive](https://isitonrecall.com/archives/) / FDA device enforcement

# APK2 Pressure-Sensing Wheelchair Cushions — FDA record Z-2593-2023

Reported ongoing

Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.

Source date Jul 6, 2023. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/).

## What the record says

- **Product**: APK2 Pressure-Sensing Wheelchair Cushions
- **Reason**: Defective battery pack in wheelchair cushions can overheat resulting in property damage and one possible injury.
- **Classification**: Class II
- **Recalling firm**: Aquila Corporation
- **Quantity**: 117 units
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-2593-2023

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2593-2023%22)

[What the recall classes mean](https://isitonrecall.com/guides/recall-classes/). Classification is an agency assessment, not individual medical advice.

## Lot and product identifiers

| Label field | Details supplied by the agency |
| --- | --- |
| Lot, code or applicability | 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 |

Match all identifying details in the current notice. A brand name alone is not enough.

## Distribution

Worldwide distribution: US (nationwide) and OUS (foreign) countries of: Canada, Sweden, Romania, Australia, UK

States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.

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## Dates in the source

- **Report date**: Sep 27, 2023
- **Recall initiation date**: Jul 6, 2023
- **Center classification date**: Sep 18, 2023

FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.

## What to do next

Read the official notice for the action that applies to your exact product.

[Read the current instructions](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2593-2023%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Aquila Corporation records](https://isitonrecall.com/brand/aquila-corporation/)
