Midmark 153901-003Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00841709107344), received between Feb 14, 2025 and Feb 14, 2025 — classified as 1 injury.

The most frequently reported specific device problem is “Device Fell” (1 report).

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.

• InjuryFeb 14, 2025Device Fell; Device Fell

  IT WAS REPORTED TO MIDMARK CORPORATION THAT ON OR AROUND (B)(6) 2025, A LED DENTAL LIGHT FELL AND HURT A STUDENT AT A DENTAL COLLEGE. THE STUDENT RECEIVED A PINCH FROM THE LIGHT. NO FURTHER DETAILS OF THE SEVERITY OF THE INJURY HAS BEEN MADE AT THE TIME OF THE INITIAL REPORT. DUE TO PREVIOUS REPORTING OF LIKE INSTANCES OF LED DENTAL LIGHTS FALLING, MIDMARK CORPORATION COMPLIED TO REPORT THIS INSTANCE.

  Patient problems: Insufficient Information

  MAUDE report 21389193 ↗