Midmark 029-7245-04Recalls & reported problems
Midmark Corporation · Trolley and track assembly used on 112 inch Midmark Dental LED Lights and Monitors. · Class 1
Data updated Oct 13, 2026 from official FDA records · Editorial policy
- 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 00841709107047), received between Aug 21, 2024 and Aug 21, 2024 — 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.
Reports received per month
Most reported problems
Device problems
- Break1
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.
MalfunctionAug 21, 2024Break; Break
IT WAS REPORTED TO MIDMARK CORPORATION THAT THE WELDMENT ON A MONITOR DOWN TUBE OF A DENTAL LIGHT BROKE, AND THE MONITOR WAS SUSPENDED BY THE WIRE HARNESS. NO USER OR PATIENT INVOLVEMENT OR INJURY REPORTED WITH THIS INSTANCE. DUE TO PREVIOUS REPORTING OF THIS OR SIMILAR LIGHT FALLING EVENTS, MIDMARK COMPLIED TO REPORT THIS INSTANCE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20016163 ↗
Other LIGHT, OPERATING, DENTAL devices
- Midmark 153905-002Midmark Corporation · LIGHT, OPERATING, DENTAL5 reports
- Midmark 029-4857-00Midmark Corporation · LIGHT, OPERATING, DENTAL3 reports
- Midmark 029-5507-00Midmark Corporation · LIGHT, OPERATING, DENTAL2 reports
- Midmark 029-4739-02Midmark Corporation · LIGHT, OPERATING, DENTAL1 report
- Midmark 153637-001Midmark Corporation · LIGHT, OPERATING, DENTAL1 report
- Midmark 153901-003Midmark Corporation · LIGHT, OPERATING, DENTAL1 report
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 13, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 13, 2026
- Page last rebuilt: Oct 13, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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