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Victory 10 LX with CTS 4 Wheel SC710LX/S710LX/IviaRecalls & reported problems

Pride Mobility Products Corp · A motorized three-wheeled vehicle is a gasoline-fueled or battery-powered device intended for medical purposes that is used for outside transportation by disabled persons. · 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 00606509300360), received between Jul 12, 2017 and Jul 16, 2025 — classified as 3 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: 0 reportsJun 2025: 0 reportsJul 2025: 1 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: 0 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 Available4
  • Fire1

Patient problems

  • Bone Fracture(s)2
  • No Known Impact Or Consequence To Patient2
  • Injury1

Recent adverse event reports

The 5 most recent of 5 reports, in the reporter's own words as published by the FDA.

  • InjuryJul 16, 2025Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available

    PROVIDER ALLEGES THE CONSUMER WAS USING THE SCOOTER AT WALMART, DISMOUNTED OFF THE SCOOTER TO REACH FOR A CABBAGE AND HELD ON TO THE SCOOTER WITH ONE HAND FOR STABILITY AND THE STEERING COLUMN OF THE SCOOTER ALLEGEDLY CAME COMPLETELY OFF THE UNIT ALLEGEDLY CAUSING THE CONSUMER TO FALL.

    Patient problems: Bone Fracture(s)

    MAUDE report 22518297 ↗
  • InjuryFeb 5, 2020Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available

    PROVIDER ALLEGES CONSUMER WAS REACHING FOR SOMETHING ON THE SHELF WHEN SHE WAS ALLEGEDLY THROWN TO THE FLOOR ON HER BACK.

    Patient problems: Injury

    MAUDE report 9670506 ↗
  • MalfunctionOct 15, 2019Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available

    PROVIDER ALLEGES END USER PUT BATTERIES ON TO CHARGE OVERNIGHT, PLUGGED INTO WALL OUTLET AND WOKE UP TO A SMOKE FILLED ROOM. FIRE DEPARTMENT WAS CALLED.

    Patient problems: No Known Impact Or Consequence To Patient

    MAUDE report 9193227 ↗
  • MalfunctionOct 9, 2018Fire; Fire

    ALLEGES AFTER RIDING SCOOTER, PLUGGED IT IN TO CHARGE AND CAME BACK OUT SHORT TIME LATER AND NOTICED SMOKE COMING FROM GARAGE. ALLEGES SCOOTER AND CHARGER CAUGHT FIRE AND HE HAD TO USE A HOSE TO PUT OUT THE FIRE.

    Patient problems: No Known Impact Or Consequence To Patient

    MAUDE report 7948119 ↗
  • InjuryJul 12, 2017Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available

    ALLEGES THE BRAKES FAILED AND THE SCOOTER FLIPPED.

    Patient problems: Bone Fracture(s)

    MAUDE report 6705701 ↗

Other Vehicle, Motorized 3-Wheeled devices

All Vehicle, Motorized 3-Wheeled devices →

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