Q6 Edge 3Recalls & 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
Quick summary
This is a Pride Mobility Q6 Edge 3 powered wheelchair, a battery-operated chair that helps people who cannot walk move around. The 86 reports mostly describe falls out of the chair, collisions, bruising and broken bones, plus a few cases of the chair catching fire while charging or moving on its own. Four reports end in death and 75 describe injuries. No recalls name this device.
AI-generated from the FDA records on this page and checked automatically against the numbers below. Read the details before relying on it.
- Adverse event reports
- 86
- Deaths reported
- 4
- Injuries reported
- 75
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 86 adverse event reports that list this exact device (DI 00606509200158), received between Sep 27, 2018 and Apr 8, 2026 — classified as 4 deaths, 75 injuries, 7 malfunctions.
The most frequently reported specific device problem is “Fire” (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. 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 Available84
- Fire1
- No Apparent Adverse Event1
- Unintended Movement1
Patient problems
- Bruise/Contusion26
- Bone Fracture(s)18
- No Clinical Signs, Symptoms or Conditions16
- Laceration(s)6
- Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available4
- Burn(s)4
- Injury4
- No Known Impact Or Consequence To Patient4
Recent adverse event reports
The 25 most recent of 86 reports, in the reporter's own words as published by the FDA.
InjuryApr 8, 2026Appropriate Device Problem Term/Code Not Available
PROVIDER STATES THE CONSUMER WAS HIT BY A CAR WHILE RIDING IN HIS UNIT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24818481 ↗InjuryMar 19, 2026Appropriate Device Problem Term/Code Not Available
PROVIDER ALLEGES THEY HAVE A CONSUMER THAT JUST GOT THIS PWC. THE CHAIR ALLEGEDLY SPARKED AND CLICKED AND THEN CAUGHT ON FIRE.
Patient problems: Burn(s)
MAUDE report 24637842 ↗InjuryDec 19, 2025Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
CONSUMER WAS HIT BY A CAR WHILE RIDING IN HER POWER CHAIR.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23848572 ↗InjuryDec 18, 2025Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
CONSUMER'S PARTNER ALLEGES THE LEFT ARM COLLAPSED ON THE UNIT ALLEGEDLY CAUSING THE CONSUMER TO FALL OUT OF CHAIR ONTO A METAL PLATE.
Patient problems: Laceration(s)
MAUDE report 23837640 ↗MalfunctionDec 15, 2025Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
PROVIDER ALLEGES THE CONSUMER WAS CHARGING HER CHAIR AT NIGHT AND ALLEGEDLY WOKE UP TO SPARKS AND FLAMES COMING FROM THE JOYSTICK.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23801601 ↗InjuryDec 4, 2025Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
PROVIDER ALLEGES CONSUMER WAS HIT BY A CAR WHILE IN THE UNIT.
Patient problems: Bruise/Contusion
MAUDE report 23714897 ↗InjuryNov 21, 2025Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
CONSUMER'S MOTHER ALLEGES HER DAUGHTER WAS IN THE CHAIR AND IT ALLEGEDLY DROVE ON ITS OWN AND RAN INTO A BOOKCASE. SHE WAS ALLEGEDLY THROWN TO THE GROUND AND THE BOOKCASE FELL ON TOP OF HER.
Patient problems: Bone Fracture(s)
MAUDE report 23616201 ↗InjuryNov 21, 2025Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
CONSUMER ALLEGES THE CHAIR TIPPED ON A LEVEL SURFACE DURING A SIMPLE LEFT TURN (NO FORWARD MOVEMENT) ALLEGEDLY CAUSING THE CONSUMER TO FALL OUT.
Patient problems: Bone Fracture(s)
MAUDE report 23616199 ↗InjuryNov 21, 2025Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
CONSUMER ALLEGES HIS UNIT TIPPED OVER WITH HIM IN IT DURING A LEFT TURN.
Patient problems: Damage to Ligament(s)
MAUDE report 23616191 ↗InjurySep 18, 2025Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
CONSUMER ALLEGES HE WAS HIT BY A CAR WHEN CROSSING THE STREET.
Patient problems: Bone Fracture(s)
MAUDE report 23083741 ↗InjuryAug 4, 2025Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
RECEIVED A LETTER FROM AN ATTORNEY THAT ALLEGES SOMETHING HAPPENED WITH THE LAP BELT (NOT CLEAR) WHICH CAUSED A FALL.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22699952 ↗InjuryAug 4, 2025Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
CONSUMER ALLEGES HE FLIPPED HIS WHEELCHAIR WHEN THE FRONT WHEEL HIT AN INDENTED AREA IN A LAWN.
Patient problems: Bruise/Contusion
MAUDE report 22699951 ↗InjuryJul 28, 2025Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
CONSUMER ALLEGES SHE WAS MOVING FORWARD IN HER CHAIR, MOVING LEFT TO RIGHT WITH PRESSURE ON THE ARMRESTS PREPARING TO TRANSFER TO HER SHOWER CHAIR WHEN ALLEGEDLY A BOLT IN THE ARMREST SNAPPED ALLEGEDLY CAUSING HER TO FALL HEADFIRST INTO THE TILED FLOOR.
Patient problems: Bone Fracture(s)
MAUDE report 22629203 ↗InjuryJun 24, 2025Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
PROVIDER ALLEGES THE BOLT BROKE WHEN THE PATIENT WAS LEADING ON THE ARMREST ALLEGEDLY CAUSING THE CONSUMER TO FALL OUT OF THE CHAIR.
Patient problems: Bone Fracture(s)
MAUDE report 22320473 ↗InjuryJun 24, 2025Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
CONSUMER ALLEGES SHE WAS ATTEMPTING TO TRANSFER ONTO THE QUANTUM CHAIR FROM HER MANUAL WHEELCHAIR. SHE WAS LEANING ON THE LEFT ARMREST WHEN IT ALLEGEDLY BROKE CAUSING THE CONSUMER TO FALL.
Patient problems: Bruise/Contusion
MAUDE report 22320256 ↗InjuryMay 16, 2025Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
CONSUMER ALLEGES THE UNIT KEPT MOVING WHEN SHE STOPPED USING IT AND SHE ALLEGEDLY HIT HER KNEE AND IT GOT IMPACTED.
Patient problems: Bruise/Contusion
MAUDE report 22034768 ↗InjuryMay 9, 2025Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
CONSUMER'S FATHER ALLEGES THE CONSUMER WAS SITTING AT HER DESK AT HER COMPUTER. THE CHAIR, ON ITS OWN ACTIVATED AND THE FOOTPADS ALLEGEDLY FORCED HER ANKLES UP WHILE HER FOOT STRAPS WERE ATTACHED AND FORCED HER ANKLES INTO A VERY PAINFUL POSITION SEVERELY STRETCHING HER CALF MUSCLE. AT THE SAME TIME HER LEGS WERE ALLEGEDLY FORCED UP AND JAMMED HER KNEES INTO THE UNDERSIDE OF THE DESK.
Patient problems: Bruise/Contusion
MAUDE report 21992151 ↗InjuryApr 24, 2025Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
CONSUMER ALLEGEDLY CUT HERSELF ON THE SEAT PAN.
Patient problems: Laceration(s)
MAUDE report 21901177 ↗DeathNov 21, 2024Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
CONSUMER WAS OPERATING THE UNIT IN THE ROADWAY (NO SIDWALK AVAILABLE) AND WAS STRUCK BY A VEHICLE
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20747884 ↗InjuryOct 29, 2024Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
PROVIDER ALLEGES CONSUMER ALLEGES THAT THE BACK BOLTS ON THE ORIGINAL BACK BROKE AND THE CONSUMER ALLEGEDLY FELL OUT OF THE CHAIR.
Patient problems: Damage to Ligament(s)
MAUDE report 20558953 ↗InjuryOct 25, 2024Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
REP ALLEGES THE TILT AND AFP ALLEGEDLY BROKE ALLEGEDLY CAUSING THE CONSUMER TO GET CAUGHT ON A THRESHOLD.
Patient problems: Laceration(s)
MAUDE report 20531857 ↗InjuryOct 25, 2024Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
PROVIDER ALLEGES CONSUMER WAS HIT BY A FED EX TRUCK WHILE IN HIS CHAIR.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20531845 ↗InjuryOct 25, 2024Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
PROVIDER ALLEGES CONSUMER WAS CROSSING A SIDE STREET IN HER POWER CHAIR AND WAS HIT BY A CAR ON LEFT SIDE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20531832 ↗InjuryOct 25, 2024Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
PROVIDER ALLEGES CONSUMER WAS RIDING IN HER UNIT WHEN HE WAS ALLEGEDLY TAPPED BY A CTA BUS AND TIPPED OVER IN HIS UNIT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20531831 ↗InjuryOct 3, 2024Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
PROVIDER ALLEGES CONSUMER ALLEGES SHE WAS DRIVING UP HER SIDE WALK TO GET INTO HER HOUSE, SHE SAID SHE GAVE THE CHAIR A COMMAND AND IT ALLEGEDLY DID NOT RESPOND, , SHE ALLEGEDLY GAVE A COUPLE MORE, SAME RESULT. THEN THE WHEELCHAIR ALLEGEDLY DROVE OFF THE SIDEWALK, ALLEGEDLY FLIPPING HER OVER INTO THE FLOWER BED.
Patient problems: Abrasion
MAUDE report 20359006 ↗
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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 16, 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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