🔍 RecallPedia

APK2 Pressure-Sensing Wheelchair Cushions

Class I - Dangerous
🏥 Medical Devices Recalled: July 6, 2023 Aquila Other Medical Devices Nationwide

What Should You Do?

  1. Check if you have this product:
    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
  2. Do not eat it: Even if it looks and smells fine, do not consume this product.
  3. Throw it away or return it: You can return the product to the store for a full refund.
  4. Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
  5. Report problems: Report any issues to the FDA's Safety Reporting Portal.

⚠️ Emergency: If you experience severe symptoms after consuming this product, call 911 or Poison Control at 1-800-222-1222.

Recall Details

Company:
Aquila Corporation
Reason for Recall:
Defective battery pack in wheelchair cushions can overheat resulting in property damage and one possible injury.
Classification:
Class I - Dangerous

Dangerous or defective products that predictably could cause serious health problems or death.

Status:
ongoing

Product Information

Full Description:

APK2 Pressure-Sensing Wheelchair Cushions

Product Codes/Lot Numbers:

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

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-2593-2023

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