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Midmark 029-4739-02Recalls & reported problems

Midmark Corporation · Monitor Flex Arm Covers Assembly used on 24 inch Midmark LED and Halogen Track Lights and Monitors. · 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 00841709106880), received between Oct 5, 2020 and Oct 5, 2020 — classified as 1 malfunction.

The most frequently reported specific device problem is “Break” (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

  • Break1
  • Therapeutic or Diagnostic Output Failure1

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 5, 2020Break; Therapeutic or Diagnostic Output Failure

    THIS REPORT SUMMARIZES <NOE>1</NOE> MALFUNCTION EVENT. THE 1 EVENT STATED THE WELD BROKE ON MONITOR MOUNT DOWN TUBE AND MONITOR WAS FOUND HANGING ON BY ITS WIRES. THE 1 EVENT REPORTED NO PATIENT, OR USER INJURY, IT BROKE BETWEEN PATIENTS.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 10626834 ↗

Other LIGHT, OPERATING, DENTAL devices

All LIGHT, OPERATING, DENTAL devices →

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