Midwest® E Pro 875110Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI E2768751100), received between Apr 23, 2024 and Oct 27, 2025 — classified as 2 malfunctions.

The most frequently reported specific device problem is “Overheating of Device” (2 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 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

• MalfunctionOct 27, 2025Overheating of Device; Overheating of Device

  THIS REPORT SUMMARIZES 1 MALFUNCTION EVENT WHERE A MIDWEST® E PRO 1:1 HANDPIECE OVERHEATED. 1 EVENT RESULTED IN NO INJURY.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 23389457 ↗
• MalfunctionApr 23, 2024Overheating of Device; Overheating of Device

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

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 19164244 ↗