Jazzy 1450Recalls & 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
- 5
- Deaths reported
- 0
- Injuries reported
- 3
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 5 adverse event reports that list this exact device (DI 00606509100021), received between Apr 26, 2018 and Jan 11, 2024 — classified as 3 injuries, 2 malfunctions.
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 Available5
Patient problems
- Injury2
- No Clinical Signs, Symptoms or Conditions2
- Abrasion1
- Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available1
Recent adverse event reports
The 5 most recent of 5 reports, in the reporter's own words as published by the FDA.
MalfunctionJan 11, 2024Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
PROVIDER ALLEGES THE CHAIR HAD A SPARK AND FIRE IN THE WIRE HARNESS.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 18494988 ↗MalfunctionMay 3, 2021Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
PROVIDER ALLEGES FORKS CAME OFF OF UNIT AND UNIT ALLEGEDLY TIPPED OVER WITH CONSUMER IN IT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 11760895 ↗InjuryJul 8, 2020Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
CONSUMER ALLEGES CHAIR MOVED ON ITS OWN ALLEGEDLY CAUSING HIM TO FALL DOWN.
Patient problems: Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available; Injury
MAUDE report 10244246 ↗InjuryJun 27, 2019Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
PROVIDER RECEIVED LETTER FROM ATTORNEY STATING CONSUMER WAS RIDING IN POWERCHAIR WHEN IT COLLAPSED, ALLEGING CONSUMER FELL TO GROUND AND SUSTAINED INJURIES. ALLEGES COMING OFF RAMP AND SEAT BROKE ALLEGEDLY FLIPPING CONSUMER BACKWARDS TO GROUND.
Patient problems: Injury
MAUDE report 8740606 ↗InjuryApr 26, 2018Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
CONSUMER'S CARE GIVER ALLEGES THAT WHEN THE CONSUMER WAS GETTING OUT OF HER CHAIR SHE ALLEGEDLY CUT HER LEFT LEG THAT RESULTED IN A HOSPITAL STAY.
Patient problems: Abrasion
MAUDE report 7463972 ↗
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.