Victory 10 DX 3 Wheel / Lunetta Victory SC610DXRecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00606509300537), received between Nov 30, 2023 and Nov 30, 2023 — classified as 1 death.

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 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

• DeathNov 30, 2023Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available

  PROVIDER ALLEGES A TRUCK COULDN'T MAKE THE TURN, THEN REVERSED WHEN THE GENTLEMAN WAS CROSSING THE CROSSWALK ALLEGEDLY RUNNING OVER THE CONSUMER.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 18236766 ↗