J6Recalls & 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
- 19
- Deaths reported
- 0
- Injuries reported
- 16
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 19 adverse event reports that list this exact device (DI 00606509100014), received between Apr 4, 2017 and May 28, 2025 — classified as 16 injuries, 3 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. How this data works · Data updated Oct 13, 2026.
Reports received per month
Most reported problems
Device problems
- Appropriate Device Problem Term/Code Not Available16
- Fire1
- Intermittent Loss of Power1
- Unintended Movement1
Patient problems
- Bone Fracture(s)4
- No Clinical Signs, Symptoms or Conditions4
- Injury3
- Abrasion1
- Bruise/Contusion1
- Contusion1
- Fracture, Arm1
- Full thickness (Third Degree) Burn1
Recent adverse event reports
The 19 most recent of 19 reports, in the reporter's own words as published by the FDA.
MalfunctionMay 28, 2025Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
PROVIDER ALLEGES THE CONSUMER ALLEGES THE RIGHT SIDE OF THE CHAIR CAUGHT ON FIRE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22095260 ↗InjuryOct 17, 2024Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
CONSUMER WAS LIFTING HER FOOTPLATE WHEN THE FOOTPLATE ALLEGEDLY CUT HER RIGHT LEG.
Patient problems: Laceration(s)
MAUDE report 20470633 ↗InjuryJan 5, 2024Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
CONSUMER ALLEGES THE CHAIR WAS NOT ORDERED WITH THE CORRECT FOOTPLATE. BECAUSE HE DOES NOT HAVE THE FOOTPLATE HIS LEG IS ALLEGEDLY DRAGGING.
Patient problems: Bruise/Contusion
MAUDE report 18451968 ↗InjuryDec 6, 2023Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
PROVIDER ALLEGES THE CONSUMER ALLEGEDLY HAD THEIR CHAIR PLUGGED IN AND SHUT OFF, THEY WERE LEANING OVER THE SIDE OF THE CHAIR DOING DISHES, ALL THE SUDDEN THE CHAIR ALLEGEDLY POWERED UP AND DROVE FORWARD INTO THE SINK. IT ALLEGEDLY PINNED THE USER'S LEGS BETWEEN THE SINK AND THE CHAIR.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 18275871 ↗InjuryMay 23, 2023Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
CONSUMER ADMITS THE ALLEGED INCIDENT WAS HIS FAULT . TWO DAYS AFTER HE RECEIVED THE UNIT . HE WAS NOT USED TO THE SENSITIVITY OF THE JOYSTICK, ALLEGEDLY RAN IT INTO THE WALL WHERE HIS FOOT ALLEGEDLY GOT CAUGHT BETWEEN THE FOOTPLATE AND THE WALL.
Patient problems: Bone Fracture(s)
MAUDE report 16983022 ↗InjuryMar 9, 2023Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
CONSUMER ALLEGES HE WAS TRANSITIONING FROM A WALKER TO HIS CHAIR. AS SOON AS HE SAT IN HIS CHAIR IT ALLEGEDLY JUST TOOK OFF AND THE CONSUMER AND THE CHAIR ALLEGEDLY WENT FULL SPEED INTO THE POOL LEVEL HOT TUB.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16514000 ↗MalfunctionJan 3, 2023Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
ALLEGES A FIRE OCCURED WHERE THE CHAIR WAS LOCATED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16088669 ↗InjuryJul 20, 2022Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
PROVIDER ALLEGES CONSUMER WENT TO GET INTO HER CHAIR WHEN HER PANT GOT HOOKED TO THE FOOT OF THE CHAIR ALLEGEDLY MAKING HER FALL ON HER LEFT SIDE.
Patient problems: Abrasion
MAUDE report 15067905 ↗InjuryJul 6, 2021Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
PROVIDER ALLEGES CONSUMER WAS LIGHTING A LIGHTER WITH AN O2 TANK MOUNTED TO BACK OF CHAIR AND ALLEGEDLY CAUGHT ON FIRE.
Patient problems: Full thickness (Third Degree) Burn; Partial thickness (Second Degree) Burn
MAUDE report 12122872 ↗InjuryApr 13, 2020Intermittent Loss of Power; Intermittent Loss of Power
CONSUMER ALLEGES SHE WAS GOING DOWN A STREET WHEN THE UNIT ALLEGEDLY CUT OUT AND SHE WAS ALLEGEDLY THROWN INTO A CEMENT STEP.
Patient problems: Injury
MAUDE report 9954556 ↗MalfunctionSep 10, 2019Fire; Fire
ALLEGES USER WAS DRIVING THE CHAIR, THE JOYSTICK CABLE WAS HANGING LOOSE, DRAGGING ALONG THE GROUND AND GOT CAUGHT IN THE REAR RIGHT CASTER WHEEL CAUSING A FIRE, BURNED THE RIGHT REAR CASTER AND JOYSTICK CABLE.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 8981385 ↗InjuryJun 27, 2019Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
ALLEGES UNIT WAS NOT FUNCTIONING PROPERLY AND CHAIR JERKED AND RAN CONSUMER INTO THE WALL CAUSING CONSUMER TO FALL OUT SUSTAINING INJURIES.
Patient problems: Bone Fracture(s)
MAUDE report 8740608 ↗InjuryOct 4, 2018Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
InjuryJul 18, 2018Unintended Movement; Unintended Movement
PROVIDER ALLEGES CONSUMER WAS REACHING FOR SOMETHING AND HER CHAIR ALLEGEDLY DROVE OFF OF THE SIDEWALK CAUSING THE CONSUMER TO ALLEGEDLY BREAK BOTH LEGS. CAREGIVER ALLEGES UNIT DRIVES ON ITS OWN.
Patient problems: Bone Fracture(s)
MAUDE report 7697836 ↗InjuryFeb 8, 2018Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
ALLEGES USER WAS ON A HILL AND GOT STUCK IN MUD. TIRES STARTED SPINNING, SO HE PUT CHAIR IN FREEWHEEL AND IT ROLLED DOWN THE HILL AND CHAIR FLIPPED OVER.
Patient problems: Fracture, Arm
MAUDE report 7251997 ↗InjuryJan 16, 2018Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
ALLEGES SITTING IN POWER CHAIR, LEANED FORWARD TO GET SOMETHING OFF OF THE END TABLE, CHAIR TIPPED FORWARD, AND FOOT GOT CAUGHT UP UNDERNEATH THE FOOTPLATES.
Patient problems: Injury
MAUDE report 7194451 ↗InjuryOct 31, 2017Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
ALLEGES USER WAS COMING TO A STOP AND SHE WAS THROWN FROM THE CHAIR BECAUSE IT TIPPED FORWARD CAUSING HER TO FALL FLAT ON HE FACE AND HURT HER THIGH.
Patient problems: Contusion
MAUDE report 6990609 ↗InjuryApr 4, 2017Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
ALLEGES CONSUMER WAS IN CHAIR WHEN IT STARTED SPINNING IN CIRCLES AND WENT UP TO LEVEL 6 BANGING HER LEG BETWEEN THE CHAIR AND HER BED.
Patient problems: No Code Available
MAUDE report 6457713 ↗InjuryApr 4, 2017Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
ALLEGES CONSUMER WAS DRIVING CHAIR IN REVERSE WHEN IT SURGED FORWARD HITTING A TABLE.
Patient problems: Bone Fracture(s)
MAUDE report 6457704 ↗
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.