Shorty Two Speed Air Motor 710024DRecalls & reported problems

Summary

The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI E276710024D0), received between Oct 23, 2024 and Apr 23, 2026 — 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. 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 3 most recent of 3 reports, in the reporter's own words as published by the FDA.

• MalfunctionApr 23, 2026Overheating of Device

  THIS REPORT SUMMARIZES 1 MALFUNCTION EVENT WHERE A MIDWEST® SHORTY® TWO SPEED AIR MOTOR (4-HOLE CONNECTION) HANDPIECES OVERHEATED. 1 EVENT RESULTED IN NO INJURY.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24964083 ↗
• MalfunctionJan 20, 2026Overheating of Device

  THIS REPORT SUMMARIZES 1 MALFUNCTION EVENT WHERE MIDWEST® SHORTY® TWO SPEED AIR MOTOR (4-HOLE CONNECTION) HANDPIECE OVERHEATED. 1 EVENT RESULTED IN NO INJURY.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 24115977 ↗
• MalfunctionOct 23, 2024Overheating of Device; Overheating of Device

  THIS REPORT SUMMARIZES 1 MALFUNCTION EVENTS WHERE A MIDWEST® SHORTY® TWO SPEED AIR MOTOR (4-HOLE CONNECTION) OVERHEATED. 1 EVENT RESULTED IN NO INJURY.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 20514166 ↗