Jazzy Elite ES/Jazzy Select Elite 2Recalls & 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
- 8
- Deaths reported
- 1
- Injuries reported
- 4
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 8 adverse event reports that list this exact device (DI 00606509100083), received between Jan 23, 2018 and Jun 18, 2026 — classified as 1 death, 4 injuries, 3 malfunctions.
The most frequently reported specific device problem is “Unintended Movement” (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 18, 2026.
Reports received per month
Most reported problems
Device problems
- Appropriate Device Problem Term/Code Not Available7
- Unintended Movement1
Patient problems
- No Clinical Signs, Symptoms or Conditions3
- Bruise/Contusion1
- Contusion1
- Damage to Ligament(s)1
- Death1
- Laceration(s)1
Recent adverse event reports
The 8 most recent of 8 reports, in the reporter's own words as published by the FDA.
MalfunctionJun 18, 2026Appropriate Device Problem Term/Code Not Available
PROVIDER ALLEGES THE CHARGER SPARKED AND CAUGHT FIRE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25545774 ↗InjuryApr 9, 2026Appropriate Device Problem Term/Code Not Available
CONSUMER ALLEGES WHEN HE FIRST RECEIVED THE UNIT HE ALLEGEDLY FELL OUT AND LANDED ON THE FLOOR HURTING HIS BACK. CONSUMER ALSO ALLEGED THIS PAST SATURDAY THE UNIT ALLEGEDLY TURNED ON ITS OWN AND HE HIT INTO A CAR.
Patient problems: Damage to Ligament(s)
MAUDE report 24832040 ↗MalfunctionMay 2, 2024Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
RECEIVED EMAIL FROM INSURANCE COMPANY THAT ALLEGES A PRIDE POWER CHAIR ALLEGEDLY CAUGHT ON FIRE AND CAUSED DAMAGE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19229000 ↗MalfunctionDec 15, 2023Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
CONSUMER ALLEGES CHARGER SPARKED THEN ALLEGEDLY CAUGHT FIRE. SHE'S CLAIMING THIS HAPPENED WHILE SHE WAS IN THE PARK. NUMOTION PICKED UP THE UNIT AND SERVICED IT BUT SHE IS HAVING CONTINUED ISSUES WITH CHARGING, POWER, TIRES, POWER INDICATOR.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 18334346 ↗InjuryMar 15, 2023Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
CONSUMER ALLEGES SHE WAS GOING THROUGH HER LIVING ROOM WHEN HER CHAIR ALLEGEDLY JERKED AND STARTED BUCKING AND ALLEGEDLY THREW HER FORWARD INTO HER FRONT DOOR.
Patient problems: Bruise/Contusion
MAUDE report 16547345 ↗InjuryJun 22, 2020Unintended Movement; Unintended Movement
CUSTOMER ALLEGES SHE SUSTAINED AN INJURY WHILE SEATED IN HER POWER CHAIR. CUSTOMER ALLEGES HER CLOTHING ACCIDENTALLY GOT CAUGHT ON THE JOYSTICK WHEN THE POWER CHAIR WAS LEFT ON RESULTING IN SUDDEN UNINTENDED MOVEMENT CAUSING THE CUSTOMER TO FORCIBLY STRIKE THE METAL FRAME OF THE HOSPITAL BED IN HER ROOM AT WARREN BARR.
Patient problems: Laceration(s)
MAUDE report 10178875 ↗DeathNov 19, 2019Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
ALLEGES CONSUMER SUFFERED SOME SYMPTOMS WHICH LIMITED HER MOBILITY AND THE USE OF THE DEVICE, SHE FELL, AND COULD NOT GET HERSELF BACK UP.
Patient problems: Death
MAUDE report 9341146 ↗InjuryJan 23, 2018Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
ALLEGES GOING TO GET ON SCOOTER AND THE LEFT ARM WOULD NOT GO DOWN AND SHE FELL.
Patient problems: Contusion
MAUDE report 7212798 ↗
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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