Midwest Tradition® Pro 790345Recalls & reported problems

Summary

The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI E2767903450), received between Jul 22, 2024 and Jul 22, 2025 — classified as 3 malfunctions.

The most frequently reported specific device problem is “Overheating of Device” (3 reports).

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 3 most recent of 3 reports, in the reporter's own words as published by the FDA.

• MalfunctionJul 22, 2025Overheating of Device; Overheating of Device

  THIS REPORT SUMMARIZES 2 MALFUNCTION EVENTS WHERE A MIDWEST E PRO 1:5 HIGH SPEED CONTRA ANGLE ATTACHMENT HANDPIECE OVERHEATED. 2 EVENTS RESULTED IN NO INJURY.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22564062 ↗
• MalfunctionOct 23, 2024Overheating of Device; Overheating of Device

  THIS REPORT SUMMARIZES 1 MALFUNCTION EVENTS WHERE A MIDWEST TRADITION® PRO TBF HANDPIECE OVERHEATED. 1 EVENT RESULTED IN NO INJURY.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 20514165 ↗
• MalfunctionJul 22, 2024Overheating of Device; Overheating of Device

  THIS REPORT SUMMARIZES 1 MALFUNCTION EVENTS WHERE A MIDWEST TRADITION® PRO TBF HANDPIECE OVERHEATED. 1 EVENT RESULTED IN NO INJURY.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 19793036 ↗