EVO614Recalls & 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
- 0
- Injuries reported
- 2
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00606509100298), received between Apr 24, 2025 and May 11, 2026 — classified as 2 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 Available2
Patient problems
- Bruise/Contusion1
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
InjuryMay 11, 2026Appropriate Device Problem Term/Code Not Available
CONSUMER'S CAREGIVER ALLEGES THE USER FELL ASLEEP WHILE IN THE CHAIR FACING A CORNER OF THE WALL WITH THEIR HAND ON THE JOYSTICK ALL NIGHT CAUSING THE PRODUCT TO RUN INTO THE WALL ALL NIGHT LONG. CAREGIVER ALLEGES IN THE MIDDLE OF THE NIGHT, THE USER HAS A DIABETIC EPISODE WHERE THE USER'S BLOOD SUGAR DROPPED SO THE USER WENT TO USE THE CHAIR TO GO GET SOMETHING FOR HER BLOOD SUGAR AND CHAIR ALLEGEDLY WOULD NOT MOVE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25134370 ↗InjuryApr 24, 2025Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
CONSUMER ALLEGES SHE WAS USING THE JAZZY ON HER RAMP, AND IT ALLEGEDLY SKID OFF THE RAMP AND SHE HIT HER KNEES.
Patient problems: Bruise/Contusion
MAUDE report 21901176 ↗
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.