Q6 Edge Z Q6 Edge Z/Q6 Edge Z with ilLevel/Q6 Ultra Sport/Q6 UltraRecalls & 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 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 4
- Deaths reported
- 0
- Injuries reported
- 4
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 00606509200073), received between Jun 1, 2020 and Aug 28, 2024 — classified as 4 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. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.
Reports received per month
Most reported problems
Device problems
- Appropriate Device Problem Term/Code Not Available4
Patient problems
- Bone Fracture(s)2
- Bruise/Contusion1
- Muscle/Tendon Damage1
Recent adverse event reports
The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.
InjuryAug 28, 2024Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
PROVIDER ALLEGES THE CONSUMER WAS LEAVING A FAST-FOOD RESTAURANT. THE CONSUMER WAS IN HIS POWER CHAIR AND WAS CROSSING A THRESHOLD. A RAMP WHICH WAS NOT SOLIDLY ATTACHED TO THE THRESHOLD WAS ALLEGEDLY PUSHED AWAY BY THE FRONT WHEELS OF THE POWER CHAIR, WHICH THEN ALLEGEDLY DUCKED DOWN IN THE SPACE BETWEEN THE THRESHOLD AND THE RAMP. THE POWER CHAIR ALLEGEDLY TILTED IN FORWARD DIRECTION AND THE OCCUPANT SLID DOWN IN FORWARD DIRECTION. THE POSITIONING BELT ALLEGEDLY COULD NOT KEEP HIS WEIGHT, AND BROKE AT THE CLASP UNDER THE STRAIN ALLEGEDLY CAUSING THE OCCUPANT TO TUMBLE FORWARD TO THE FLOOR.
Patient problems: Bone Fracture(s)
MAUDE report 20087364 ↗InjuryJan 11, 2024Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
PROVIDER ALLEGES THE CONSUMER WAS ON THE SECOND LEVEL OF ERIN MILLS TOWN CENTRE NEAR THE ESCALATOR IN HIS QUANTUM Q6 EDGE WHEELCHAIR, WHEN SUDDENLY AND WITHOUT WARNING, HIS WHEELCHAIR AND/OR THE ESCALATOR ALLEGEDLY MALFUNCTIONED AND ALLEGEDLY CAUSED HIM TO FALL DOWN THE ESCALATOR.
Patient problems: Bruise/Contusion
MAUDE report 18494978 ↗InjurySep 24, 2020Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
ALLEGES TRYING TO NAVIGATE A SIMPLE TRANSITION FROM SIDEWALK TO ROAD WHEN THE MOTOR ASSEMBLY ON THE ONE SIDE LOST POWER AND THE OTHER CONTINUED TO GO CAUSING THE CHAIR TO SPIN TO ONE SIDE AND THROW CUSTOMER INTO THE STREET.
Patient problems: Muscle/Tendon Damage
MAUDE report 10579278 ↗InjuryJun 1, 2020Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
ALLEGES THE CHAIR SUDDENLY STOPPED, TIPPED FORWARD WITHOUT TILTING COMPLETELY, CUSTOMER'S FEET HIT THE GROUND, AND CAUSED INJURY.
Patient problems: Bone Fracture(s)
MAUDE report 10105395 ↗
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 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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