Midmark 029-5507-00Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00841709106903), received between Jul 18, 2023 and Jun 19, 2026 — classified as 2 malfunctions.

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

• MalfunctionJun 19, 2026Device Fell

  IT WAS REPORTED TO MIDMARK CORPORATION THAT A DENTAL LIGHT POST CAME UNTHREADED FROM THE TROLLEY AND FELL ONTO PATIENT IN CHAIR. IT HIT THE PATIENT IN THE LEG. NO INJURY OCCURRED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 25565561 ↗
• MalfunctionJul 18, 2023Device Fell; Device Fell

  THIS REPORT SUMMARIZES 1 EVENT. THE 1 EVENT REPORTED TO MIDMARK CORPORATION WAS THAT THE LIGHT FLEX ARM HOLDING A MONITOR DETACHED FROM THE CEILING MOUNT TRACK DURING ADJUSTMENT OF THE DEVICE. NO PATIENT OR INJURY WAS INVOLVED IN THIS EVENT. DUE TO PREVIOUS REPORTING OF THIS OR SIMILAR EVENTS, MIDMARK CORPORATION COMPLIED TO REPORT THIS INSTANCE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 17340930 ↗