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Midmark 255-023Recalls & reported problems

Midmark Corporation · The Midmark 8' Dual 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 00841709106828), received between Sep 21, 2023 and Sep 21, 2023 — 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.

  • MalfunctionSep 21, 2023Device Fell; Device Fell

    THIS REPORT SUMMARIZES 1 EVENT. THE 1 EVENT REPORTED TO MIDMARK CORPORATION WAS THAT A LIGHT ARM OF A DUAL CEILING LIGHT DETACHED AT THE BALL JOINT AND FELL. NO PATIENT OR INJURY WAS INVOLVED IN THIS EVENT. DUE TO REPORTING OF THIS OR SIMILAR EVENTS, MIDMARK CORPORATION COMPLIED TO REPORT THIS INSTANCE.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 17789969 ↗

Other Device, medical examination, ac powered devices

All Device, medical examination, ac powered devices →

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