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Jazzy Elite 14Recalls & 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
9
Deaths reported
0
Injuries reported
7
Recalls naming it
0

Summary

The FDA's MAUDE database contains 9 adverse event reports that list this exact device (DI 00606509100076), received between Dec 22, 2017 and May 20, 2026 — classified as 7 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.

Reports received per month

Nov 2023: 0 reportsDec 2023: 0 reportsJan 2024: 0 reportsFeb 2024: 0 reportsMar 2024: 0 reportsApr 2024: 0 reportsMay 2024: 0 reportsJun 2024: 0 reportsJul 2024: 0 reportsAug 2024: 0 reportsSep 2024: 0 reportsOct 2024: 0 reportsNov 2024: 0 reportsDec 2024: 0 reportsJan 2025: 0 reportsFeb 2025: 0 reportsMar 2025: 0 reportsApr 2025: 0 reportsMay 2025: 1 reportsJun 2025: 0 reportsJul 2025: 0 reportsAug 2025: 0 reportsSep 2025: 0 reportsOct 2025: 0 reportsNov 2025: 0 reportsDec 2025: 0 reportsJan 2026: 0 reportsFeb 2026: 0 reportsMar 2026: 0 reportsApr 2026: 0 reportsMay 2026: 1 reportsJun 2026: 0 reportsJul 2026: 0 reportsAug 2026: 0 reportsSep 2026: 0 reportsOct 2026: 0 reports2024202520261
Last 36 months. The most recent month may be incomplete.

Most reported problems

Device problems

  • Appropriate Device Problem Term/Code Not Available8
  • Fire1

Patient problems

  • Bruise/Contusion2
  • Abrasion1
  • Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available1
  • Bone Fracture(s)1
  • Injury1
  • No Clinical Signs, Symptoms or Conditions1
  • No Information1
  • No Known Impact Or Consequence To Patient1

Recent adverse event reports

The 9 most recent of 9 reports, in the reporter's own words as published by the FDA.

  • InjuryMay 20, 2026Appropriate Device Problem Term/Code Not Available

    CONSUMER IS ALLEGING THE UNIT THREW HIM OUT OF THE CHAIR AND HE ALLEGEDLY HIT HIS HEAD.

    Patient problems: Bruise/Contusion

    MAUDE report 25228231 ↗
  • InjuryMay 9, 2025Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available

    CONSUMER ALLEGES THAT THE UNIT NO LONGER HAVE A SLOW SPEED, WHICH ALLEGEDLY CAUSED HER TO BE THROWN FROM THE UNIT.

    Patient problems: Bruise/Contusion

    MAUDE report 21992153 ↗
  • MalfunctionSep 26, 2022Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available

    PROVIDER ALLEGES THE UNIT CAUGHT FIRE WHILE CHARGING IN THE BEDROOM.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 15484805 ↗
  • InjuryAug 8, 2022Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available

    CONSUMER ALLEGES HE WAS RIDING IN HIS CHAIR WHEN THE JOYSTICK BECAME WOBBLY AND ALLEGEDLY RAN HIM OFF THE SIDEWALK AND ALLEGEDLY ENDED UP FACE DOWN ON THE HIGHWAY.

    Patient problems: Bone Fracture(s)

    MAUDE report 15183218 ↗
  • InjuryJun 21, 2021Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available

    ALLEGES CUSTOMER WAS THROWN FROM DEVICE WHEN IT CUT OUT AND STOPPED.

    Patient problems: Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available

    MAUDE report 12031448 ↗
  • InjuryFeb 14, 2019Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available

    ALLEGES CUSTOMER DROVE DOWN A FLIGHT OF FIFTEEN (15) STAIRS.

    Patient problems: Injury

    MAUDE report 8339259 ↗
  • MalfunctionJun 15, 2018Fire; Fire

    ALLEGES CHARGER CAUGHT ON FIRE.

    Patient problems: No Known Impact Or Consequence To Patient

    MAUDE report 7605280 ↗
  • InjuryApr 26, 2018Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available

    PROVIDER ALLEGES CONSUMER WAS RIDING ON A SIDEWALK WHEN THE UNIT ALLEGEDLY PULLED HARD TO THE SIDE CAUSING HIM TO GO OFF OF THE CURB. THE CHAIR ALLEGEDLY TIPPED OVER CAUSING THE CONSUMER TO FALL OUT AND THE UNIT TO LAND ON TOP OF HIM.

    Patient problems: Abrasion

    MAUDE report 7463967 ↗
  • InjuryDec 22, 2017Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available

    CLAIMS WAS HIT BY A CAR FROM BEHIND AND WAS THROWN FROM THE CHAIR.

    Patient problems: No Information

    MAUDE report 7141850 ↗

Other Wheelchair, Powered devices

All Wheelchair, Powered devices →

Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.