Jazzy Select 6Recalls & 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 13, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 13
- Deaths reported
- 0
- Injuries reported
- 11
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 13 adverse event reports that list this exact device (DI 00606509100137), received between Mar 2, 2017 and Dec 7, 2021 — classified as 11 injuries, 2 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.
Most reported problems
Device problems
- Appropriate Device Problem Term/Code Not Available11
- Fire1
- Unintended Movement1
Patient problems
- Abrasion2
- Bone Fracture(s)2
- Injury2
- No Code Available2
- Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available1
- Bruise/Contusion1
- Hip Fracture1
- Neck Pain1
Recent adverse event reports
The 13 most recent of 13 reports, in the reporter's own words as published by the FDA.
InjuryDec 7, 2021Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
CONSUMER ALLEGES HER RIGHT LEG GOT CAUGHT BETWEEN THE LIFTED FOOT PLATFORM AND WHEEL ALLEGEDLY CAUSING HER TO FALL.
Patient problems: Bone Fracture(s)
MAUDE report 12951585 ↗InjuryJul 19, 2021Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
CONSUMER'S HUSBAND ALLEGES HIS WIFE WAS CROSSING THE STREET IN HER CHAIR WHEN SHE WAS ALLEGEDLY HIT BY A CAR.
Patient problems: Bone Fracture(s); Hip Fracture
MAUDE report 12189528 ↗InjuryJun 7, 2021Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
CONSUMER ALLEGES THEY WERE GOING ALONG A SIDEWALK AND THE CHAIR ALLEGEDLY KEPT GOING TO THE RIGHT WHEN SHE ALLEGEDLY WENT OFF A CURB AND FELL OUT.
Patient problems: Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available
MAUDE report 11945957 ↗MalfunctionMar 1, 2021Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
ALLEGES WHILE RIDING THE CHAIR AND SMOKING A CIGARETTE, BUMPED INTO A KEROSENE HEATER, AND CAUGHT THE CHAIR ON FIRE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 11392504 ↗InjuryOct 12, 2020Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
ALLEGES THE ARM OF THE UNIT THAT HOLDS THE JOYSTICK KEEPS POPPING OFF AND WHEN HITTING A BUMP THE CHAIR TOPPLED OVER WITH END USER IN IT AND THE PARAMEDICS WERE CALLED.
Patient problems: Abrasion
MAUDE report 10661047 ↗InjuryAug 31, 2020Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
CONSUMER'S WIFE ALLEGES CONSUMER WAS GOING DOWN A RAMP WHEN HIS CHAIR ALLEGEDLY SPED UP AND WENT OFF RAMP.
Patient problems: Bruise/Contusion
MAUDE report 10474676 ↗InjuryJul 13, 2020Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
PROVIDER ALLEGES ISSUES WITH THE MOTORS ALLEGEDLY CAUSED THE UNIT TO COME TO A STOP THROWING THE CONSUMER OUT.
Patient problems: Pain
MAUDE report 10264123 ↗InjuryDec 17, 2019Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
CONSUMER ALLEGES WHILE SHE WAS ON A BUS HER CHAIR ALLEGEDLY TIPPED OVER AND SHE HIT HER HEAD ON THE WINDOW.
Patient problems: Neck Pain; Sprain
MAUDE report 9482339 ↗InjurySep 10, 2019Unintended Movement; Unintended Movement
ALLEGES WAS GOING DOWN THE LEVEL PUBLIC SIDEWALK WHEN THE CHAIR JERKED AND SPUN OUT, THROWING HIS WEIGHT TO ONE SIDE AND THE CHAIR WENT DOWN AS DID CUSTOMER CAUSING INJURIES.
Patient problems: Injury
MAUDE report 8981387 ↗InjuryJun 27, 2019Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
CONSUMER ALLEGES A CAR RAN OVER HER FOOT THEN RAN OVER THE SEAT OF HER CHAIR.
Patient problems: Injury
MAUDE report 8740610 ↗MalfunctionJul 3, 2018Fire; Fire
CONSUMER ALLEGES HIS HOUSE CAUGHT ON FIRE WITH THE UNIT INSIDE.
Patient problems: No Code Available
MAUDE report 7658637 ↗InjuryNov 9, 2017Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
ALLEGES THE TURN SPEED CAUSED CONSUMER TO RUN INTO A WALL. ALLEGES MOTIONING TO TURN THE CHAIR OFF BUT APPARENTLY CAUGHT HIS SLEEVE ON OR BRUSHED AGAINST THE JOYSTICK WITH HIS WRIST. THE CHAIR ACCELERATED QUICKLY PINNING HIS LEGS AGAINST DRESSER AND CUT HIS LEG.
Patient problems: Abrasion
MAUDE report 7013029 ↗InjuryMar 2, 2017Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
PROVIDER ALLEGES THE CONSUMER LET GO OF THE JOYSTICK, THE UNIT KEPT MOVING, AND ALLEGEDLY PINNED THE CONSUMER AGAINST HIS ENTERTAINMENT CENTER. CONSUMER CALLED 911.
Patient problems: No Code Available
MAUDE report 6371825 ↗
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 13, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 13, 2026
- Page last rebuilt: Oct 13, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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