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Midmark 255-021Recalls & reported problems

Midmark Corporation · The Midmark 8' Single Ceiling Mount LED Procedure Light is intended to be used in medical environments where illumination is required for medical use during external examinations and procedures. · Class 1

Adverse event reports
1
Deaths reported
0
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00841709106804), received between Oct 22, 2021 and Oct 22, 2021 — 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

Device problems

  • Device Fell1

Patient problems

  • No Clinical Signs, Symptoms or Conditions1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • MalfunctionOct 22, 2021Device Fell; Device Fell

    THIS REPORT SUMMARIZES 1 MALFUNCTION EVENT THAT OCCURRED ON OR ABOUT (B)(6) 2021 PER NOTICE TO MIDMARK. IT WAS STATED THAT A MODEL 255 PROCEDURE LIGHT HEAD FELL FROM THE CEILING DUE TO STRIPPED OR BROKEN BOLTS. NO INJURY WAS REPORTED WITH THIS INSTANCE.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 12679906 ↗

Other Device, medical examination, ac powered devices

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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.