FDA Device recall Z-2594-2023

SofTech Pressure-Sensing Wheelchair Cushions

FDA Device
Class II
ongoing
Published 2023-09-27

On 2023-09-27 the FDA classified a Class II recall of SofTech Pressure-Sensing Wheelchair Cushions by Aquila, citing defective battery pack in wheelchair cushions can overheat resulting in property damage and one possible injury.

Read the official FDA Device notice

Agency	FDA Device
Recall number	Z-2594-2023
Classification	Class II
Status	ongoing
Initiated	2023-07-06
Published	2023-09-27
Last updated	2026-09-13 11:56 UTC
Company	Aquila
Distribution	US

Product

SofTech Pressure-Sensing Wheelchair Cushions

Reason

Defective battery pack in wheelchair cushions can overheat resulting in property damage and one possible injury.

Identifiers

code_info	Serial Numbers: 4441, 4541, 5064, 5681, 6012, 6078, 6342, 6487, 6547, 6835, 6844, 6859, 6869, 6976, 6985, 6989, 6990,… 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

code_info

Serial Numbers: 4441, 4541, 5064, 5681, 6012, 6078, 6342, 6487, 6547, 6835, 6844, 6859, 6869, 6976, 6985, 6989, 6990,…

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

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: ongoing.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2594-2023%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.