Midmark 153637-001Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00841709107092), received between Aug 23, 2024 and Aug 23, 2024 — classified as 1 malfunction.

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.

• MalfunctionAug 23, 2024Device Fell; Device Fell

  IT WAS REPORTED TO THE MIDMARK CORPORATION THAT A DENTAL CEILING LIGHT FELL FROM THE CEILING MOUNT. NO PATIENT OR USER INVOLVEMENT WAS REPORTED. DUE TO PREVIOUS REPORTING OF THIS OR SIMILAR LIGHT FALLING EVENTS, MIDMARK CORPORATION COMPLIED TO REPORT THIS INSTANCE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 20048246 ↗