Universal Light Guide Adapter OLYMPUS MAJ-1200Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 04953170155017), received between Jun 17, 2021 and Jun 17, 2021 — classified as 1 malfunction.

The most frequently reported specific device problem is “Defective Device” (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. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.

Most reported problems

Recent adverse event reports

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

• MalfunctionJun 17, 2021No Device Output; Defective Device; Electrical Power Problem; No Device Output; Defective Device; Electrical Power Problem

  IT WAS REPORTED THAT THE DEVICE DOES NOT TURN ON, THE XENON LAMP AND THE EMERGENCY LAMP DOES NOT WORK. THE POWER INPUT CARD AND TRANSFORMER ARE ALTERED BY A THIRD PARTY. THE ISSUE FOUND DURING AN UNKNOWN EVENT. NO PATIENT INVOLVEMENT REPORTED, NO USER INJURY REPORTED DUE TO THE EVENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 12018039 ↗