---
title: "SofTech Pressure-Sensing Wheelchair Cushions — FDA record Z-2594-2023 | 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-2594-2023-softech-pressure-sensing-wheelchair-cushions/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

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

# SofTech Pressure-Sensing Wheelchair Cushions — FDA record Z-2594-2023

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**: SofTech 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**: 134 units
- **Agency-reported status**: Ongoing
- **Source record identifier**: Z-2594-2023

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2594-2023%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: 4441, 4541, 5064, 5681, 6012, 6078, 6342, 6487, 6547, 6835, 6844, 6859, 6869, 6976, 6985, 6989, 6990, 6994, 6994, 6995, 6995, 6996, 6997, 7001, 7002, 7016, 7017, 7018, 7021, 7022, 7022, 7023, 7023, 7031, 7033, 7058, 7059, 7059, 7060, 7061, 7061, 7065, 7066, 7074, 7075, 7076, 7076, 7077, 7080, 7080, 7081, 7081, 7082, 7083, 7084, 7521, 7599, 7774, 7774, 7854, 7862, 7863, 7864, 7864, 7871, 7871, 7873, 7873, 7874, 7876, 7881, 7883, 7885, 7886, 7887, 7887, 7893, 7896, 7904, 7905, 7907, 7929, 7930, 7930, 7932, 7934, 7936, 7939, 7939, 7940, 7941, 7941, 7942, 7943, 7943, 7951, 7952, 7956, 7956, 7970, 7971, 7971, 7973, 7974, 7979, 7980, 7981, 7981, 7982, 7988, 7988, 7989, 7990, 7993, 7993, 7996, 7997, 7997, 7999, 8000, 8001, 8002, 8003, 8003, 8004, 8005, 8006, 8007, 8008, 8010, 8011, 8012, 8013, 8044 |

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-2594-2023%22)

## Related records

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