Maxima 4 Wheel SC941Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00606509300551), received between Jul 20, 2022 and Nov 16, 2022 — classified as 2 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. How this data works · Data updated Oct 13, 2026.

Most reported problems

Recent adverse event reports

The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

• InjuryNov 16, 2022Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available

  PROVIDER ALLEGES CONSUMER WAS DRIVING DOWN A SIDEWALK WHEN THE WELD ON THE SEAT POST ALLEGEDLY BROKE ALLEGEDLY CAUSING THE CONSUMER TO FALL OUT OF THE CHAIR.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 15805340 ↗
• InjuryJul 20, 2022Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available

  PROVIDER ALLEGES CONSUMER HIT A PEBBLE AND THE STEERING WAS ALLEGEDLY OFF. THE SCOOTER ALLEGEDLY TOOK OFF AND FLIPPED OVER WITH THE CONSUMER IN IT.

  Patient problems: Bone Fracture(s)

  MAUDE report 15067795 ↗