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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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High RiskFDA Device
Medical Devices/Home Healthcare

Aquila Corporation: Pressure-Sensing Wheelchair Cushions Recalled for Overheating Battery Packs

Agency Publication Date: September 18, 2023
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Summary

Aquila Corporation has recalled 251 APK2 and SofTech Pressure-Sensing Wheelchair Cushions because a defective battery pack can overheat. This defect has already caused property damage and one reported injury. These specialized cushions were distributed worldwide and in the United States, including specific serial numbers manufactured in the U.S. and sold across various regions.

Risk

The cushion's internal battery pack is defective and can overheat during use or charging. This creates a fire hazard that can lead to property damage and serious burns or other injuries to the user.

What You Should Do

  1. Check your wheelchair cushion to see if it is an APK2 or SofTech model manufactured by Aquila Corporation.
  2. Verify your specific serial number against the list of affected units. For APK2 cushions, look for 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, 6903, 6949, 6967, 6983, 6988, 6991, 6992, 6993, 6998, 6999, 7003, 7012, 7013, 7014, 7015, 7019, 7024, 7027, 7028, 7029, 7034, 7035, 7036, 7037, 7056, 7057, 7063, 7064, 7078, 7087, 7088, 7090, 7504, 7515, 7619, 7673, 7696, 7725, 7764, 7782, 7838, 7867, 7869, 7877, 7878, 7879, 7880, 7884, 7888, 7889, 7890, 7891, 7901, 7902, 7903, 7937, 7945, 7946, 7947, 7948, 7953, 7954, 7955, 7975, 7976, 7977, 7991, 7992.
  3. For SofTech cushions, check for serial numbers: 4441, 4541, 5064, 5681, 6012, 6078, 6342, 6487, 6547, 6835, 6844, 6859, 6869, 6976, 6985, 6989, 6990, 6994, 6995, 6996, 6997, 7001, 7002, 7016, 7017, 7018, 7021, 7022, 7023, 7031, 7033, 7058, 7059, 7060, 7061, 7065, 7066, 7074, 7075, 7076, 7077, 7080, 7081, 7082, 7083, 7084, 7521, 7599, 7774, 7854, 7862, 7863, 7864, 7871, 7873, 7874, 7876, 7881, 7883, 7885, 7886, 7887, 7893, 7896, 7904, 7905, 7907, 7929, 7930, 7932, 7934, 7936, 7939, 7940, 7941, 7942, 7943, 7951, 7952, 7956, 7970, 7971, 7973, 7974, 7979, 7980, 7981, 7982, 7988, 7989, 7990, 7993, 7996, 7997, 7999, 8000, 8001, 8002, 8003, 8004, 8005, 8006, 8007, 8008, 8010, 8011, 8012, 8013, 8044.
  4. If your cushion is affected, stop using the product and contact Aquila Corporation at 1-608-782-0031 or visit their website at www.aquilacorp.com for instructions on receiving a replacement battery pack.
  5. Contact your healthcare provider if you have concerns about skin health or alternative seating while the cushion is being repaired.
  6. For additional questions, contact the FDA at 1-888-463-6332 (1-888-INFO-FDA) or visit www.fda.gov/medical-devices/medical-device-recalls.

Your Remedy Options

๐Ÿ“‹Other Action

Battery pack replacement and instructions

How to: Contact your healthcare provider or the manufacturer (Aquila Corporation) for further instructions and potential refund

Affected Products

Product: APK2 Pressure-Sensing Wheelchair Cushions
Model / REF:
Z-2593-2023
Lot Numbers (93):
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
6903
6949
6967
6983
6988
6991
6992
6993
6998
6999
7003
7012
7013
7014
7015
7019
7024
7027
7028
7029
7034
7035
7036
7037
7056
Product: SofTech Pressure-Sensing Wheelchair Cushions
Model / REF:
Z-2594-2023
Lot Numbers (109):
4441
4541
5064
5681
6012
6078
6342
6487
6547
6835
6844
6859
6869
6976
6985
6989
6990
6994
6995
6996
6997
7001
7002
7016
7017
7018
7021
7022
7023
7031
7033
7058
7059
7060
7061
7065
7066
7074
7075
7076
7077
7080
7081
7082
7083
7084
7521
7599
7774
7854

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 92790
Status: Active
Manufacturer: Aquila Corporation
Sold By: Aquila Corporation; authorized medical device distributors
Manufactured In: United States
Units Affected: 2 products (117 units; 134 units)
Distributed To: Nationwide

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

Find an Attorney

This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES ยท Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.