J4E HDRecalls & 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
- 2
- Deaths reported
- 1
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00606509200257), received between Mar 5, 2026 and Apr 21, 2026 — classified as 1 death, 1 injury.
The most frequently reported specific device problem is “Defective Component” (1 report).
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 Available1
- Defective Component1
- Self-Activation or Keying1
Patient problems
- Laceration(s)1
- Multiple Organ Dysfunction Syndrome1
- Paralysis1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
DeathApr 21, 2026Self-Activation or Keying; Defective Component
IT IS ALLEGED THE JOYSTICK OF A WHEELCHAIR EXECUTED AN UNCOMANDED 90 TO 0 DEGREE RECLINE WHICH RESULTED IN FATAL LUMBER INJURY.
Patient problems: Multiple Organ Dysfunction Syndrome; Paralysis
MAUDE report 24938123 ↗InjuryMar 5, 2026Appropriate Device Problem Term/Code Not Available
CONSUMER ALLEGES THE UNIT/SEAT SIZE IS TOO SMALL FOR BODY TYPE. THE ARMREST IS TOO SHORT AND REQUIRING CUSTOMER TO CURL WRIST TO USE CONTROL. CONSUMER ALLEGES SHE HAD SMASHED HER LEG ON A DOOR AND KNICKED HER WRIST.
Patient problems: Laceration(s)
MAUDE report 24518940 ↗
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.