Quantum Rival R44/Lightning/Rival RQ/Partner/Lightning EVORecalls & 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
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 9
- Deaths reported
- 0
- Injuries reported
- 7
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 9 adverse event reports that list this exact device (DI 00606509200134), received between Jan 16, 2018 and Sep 26, 2024 — classified as 7 injuries, 2 malfunctions.
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. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.
Reports received per month
Most reported problems
Device problems
- Appropriate Device Problem Term/Code Not Available9
Patient problems
- Bone Fracture(s)6
- No Known Impact Or Consequence To Patient2
- Abrasion1
- Bruise/Contusion1
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 9 most recent of 9 reports, in the reporter's own words as published by the FDA.
InjurySep 26, 2024Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
CONSUMER'S DAUGHTER ALLEGES SHE WENT FOR A WALK WITH HER MOTHER AROUND HER HOUSE AND WHEN THEY WERE GOING DOWN A STREET THE CHAIR ALLEGEDLY DID NOT STOP AND ALLEGEDLY BEGAN TO ROLL DOWNHILL ON ITS OWN. CONSUMER ALLEGES HER MOTHER SHOUTED THAT THE CHAIR DID NOT STOP. CONSUMER'S DAUGHTER RAN TO TRY TO STOP IT AND SHE ONLY MANAGED TO STOP IT A LITTLE BUT THE CHAIR WENT AGAINST THE CURB AND CONSUMER'S MOTHER ALLEGEDLY FELL OFF THE CHAIR.
Patient problems: Bone Fracture(s)
MAUDE report 20310533 ↗InjuryAug 24, 2023Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
PROVIDER ALLEGES CONSUMER ALLEGES SHE STRUCK A WALL WHILE IN HER UNIT ALLEGEDLY BREAKING HER LEG/FOOT.
Patient problems: Bone Fracture(s)
MAUDE report 17611711 ↗InjuryJun 13, 2022Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
PROVIDER ALLEGES CONSUMER WAS GOING DOWN THE SIDEWALK WHEN THE BOLT/NUT ALLEGEDLY CAME OFF THE POWER WHEELCHAIR TIRE/CASTER FORK ALLEGEDLY CAUSING THE CONSUMER TO FALL OUT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 14676191 ↗InjuryJun 2, 2022Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
CONSUMER ALLEGES THE ARMREST MOVED ON HIM AND HIS ARM ALLEGEDLY FELL BETWEEN THE BED AND THE CHAIR.
Patient problems: Bone Fracture(s)
MAUDE report 14577530 ↗InjuryAug 23, 2021Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
ALLEGES BEING HIT BY A VEHICLE WHILE IN POWERCHAIR.
Patient problems: Abrasion; Bone Fracture(s); Bruise/Contusion
MAUDE report 12353737 ↗MalfunctionJun 8, 2020Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
PROVIDER ALLEGES THE CONSUMER'S UNIT ALLEGEDLY SHUT OFF AND THREW HIM FROM THE UNIT.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 10128395 ↗MalfunctionMay 18, 2020Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
WHILE RIDING IN THE CHAIR THE FRONT CASTER WHEEL ALLEGEDLY BROKE AND THE CONSUMER ALLEGEDLY FELL OUT OF THE CHAIR.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 10065844 ↗InjuryMar 25, 2019Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
RECEIVED A LETTER FROM AN ATTORNEY ALLEGING HIS CLIENT SUSTAINED INJURIES DUE TO AN ALLEGED MALFUNCTION.
Patient problems: Bone Fracture(s)
MAUDE report 8447806 ↗InjuryJan 16, 2018Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
ALLEGES CROSSING STREET IN CHAIR WHEN A DRIVER RAN A STOP SIGN AND HIT CONSUMER.
Patient problems: Bone Fracture(s)
MAUDE report 7195436 ↗
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 and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 13, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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