Go Go Ultra X 3 Wheel SC40X/S40X/Beaufort 3Recalls & reported problems

Summary

The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 00606509300223), received between Oct 31, 2017 and Aug 10, 2022 — classified as 4 injuries.

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.

Most reported problems

Recent adverse event reports

The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.

• InjuryAug 10, 2022Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available

  ALLEGES SHE WAS BACKING UP ON A SIDEWALK AND THE BACK WHEEL WENT OFF THE SIDEWALK INTO THE GRASS ALLEGEDLY CAUSING THE SCOOTER TO LEAN TO ONE SIDE AND TIP OVER.

  Patient problems: Bruise/Contusion

  MAUDE report 15198298 ↗
• InjuryJul 6, 2021Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available

  CONSUMER ALLEGES THE SCOOTER THREW HIM OFF. CONSUMER ALSO ALLEGES IT TURNS TOO FAST.

  Patient problems: Abrasion; Laceration(s)

  MAUDE report 12122894 ↗
• InjuryOct 2, 2018Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available

  ALLEGES END USER BACKED OFF A CURB AND SUSTAINED INJURY.

  Patient problems: Bone Fracture(s)

  MAUDE report 7926049 ↗
• InjuryOct 31, 2017Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available

  ALLEGES CUSTOMER WAS USING UNIT AT HOME AND FELL OFF. CLAIMS THE SPEED POT DIAL/KNOB IS TOO EASY TO TURN. CLAIMS THERE IS PLAY WHERE THE SEAT AND SEAT POST MEET.

  Patient problems: Contusion

  MAUDE report 6990607 ↗