J4Recalls & reported problems
Pride Mobility Products Corp · A powered wheelchair is a battery-operated device with wheels that is intended for medical purposes to provide mobility to persons restricted to a sitting position. · Class 2
- Adverse event reports
- 5
- Deaths reported
- 0
- Injuries reported
- 5
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 5 adverse event reports that list this exact device (DI 00606509100243), received between Nov 16, 2022 and Oct 27, 2025 — classified as 5 injuries.
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. How this data works · Data updated Oct 13, 2026.
Reports received per month
Most reported problems
Device problems
- Appropriate Device Problem Term/Code Not Available5
Patient problems
- Bruise/Contusion2
- No Clinical Signs, Symptoms or Conditions2
- Laceration(s)1
Recent adverse event reports
The 5 most recent of 5 reports, in the reporter's own words as published by the FDA.
InjuryOct 27, 2025Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
CONSUMER ALLEGES THAT WHILE USING HIS CHAIR, IT ALLEGEDLY "BECAME POSSESSED AND SPED UP" ALLEGEDLY RESULTING IN HIM CRASHING INTO HIS CUPBOARD.
Patient problems: Laceration(s)
MAUDE report 23392903 ↗InjuryMay 16, 2025Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
CONSUMER ALLEGES HE WAS RECLINED BACK IN HIS QUANTUM J4 CHAIR AND ACCIDENTLY HIT THE JOYSTICK AND CHAIR ALLEGEDLY TIPPED OVER.
Patient problems: Bruise/Contusion
MAUDE report 22034769 ↗InjuryJan 30, 2025Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
CONSUMER'S COUSIN ALLEGES WHILE THE CONSUMER WAS ELEVATING HER SEAT, FRAME ALLEGEDLY GAVE WAY AND CONSUMER CAME CRASHING DOWN.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21273643 ↗InjuryFeb 29, 2024Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
RECEIVED NOTICE FROM AN ATTORNEY ABOUT AN ALLEGED INCIDENT THAT TOOK PLACE REGARDING THE ARMRESTS OF THE CONSUMER'S UNIT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 18807679 ↗InjuryNov 16, 2022Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
PROVIDER ALLEGES CONSUMER WENT TO SHIFT HIS WEIGHT PUSHING ON THE ARMS WHEN THE L BRACKET THAT HOLDS THE STOP ON THE ARMREST ALLEGEDLY BROKE ALLEGEDLY CAUSING THE CONSUMER TO FALL OUT.
Patient problems: Bruise/Contusion
MAUDE report 15807434 ↗
Other Wheelchair, Powered devices
- SmartDrive® MX2+Max Mobility, LLC · Wheelchair, Powered858 reports
- Permobil M3Permobil, Inc. · Wheelchair, Powered1 recall59 reports
- TDX SP2 Base for Multiple Actuator System w/ Ultra Low Maxx TDXSP2-MCGInvacare Corporation · Wheelchair, powered2 recalls2 reports
- TDX SP2 with LiNX Electronics TDXSP2Invacare Corporation · Wheelchair, powered2 recalls0 reports
- Invacare® TDX SP2 with Captain's Seat TDXSP2VInvacare Corporation · Wheelchair, powered2 recalls0 reports
- Q6 Edge 3Pride Mobility Products Corp · Wheelchair, Powered4 deaths86 reports
- Q6 Edge 2.0 Q6 Edge 2.0 / Q6 Edge 2.0 with iLevelPride Mobility Products Corp · Wheelchair, Powered1 death83 reports
- Permobil M5Permobil, Inc. · Wheelchair, Powered1 recall7 reports
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.