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4K Cable 22M MAJ-2255Recalls & reported problems

Olympus Medical Systems Corp. · Class 2

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 04953170374692), received between Jan 10, 2021 and Jan 10, 2021 — classified as 1 malfunction.

The most frequently reported specific device problem is “Defective Component” (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

  • Defective Component1

Patient problems

  • No Patient Involvement1

Recent adverse event reports

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

  • MalfunctionJan 10, 2021Defective Component; Defective Component

    IT IS REPORTED DURING PREPARATION FOR USE, A VISERA 4K UHD XENON LIGHT SOURCE WAS FOUND TO HAVE A MICROSWITCH THAT ACTIVATES THE HIGH INTENSITY NOT WORKING. THERE WAS NO PATIENT CONTACT/IMPACT RELATED TO THIS OCCURRENCE.

    Patient problems: No Patient Involvement

    MAUDE report 11144241 ↗

Other Endoscope, accessories, narrow band spectrum devices

All Endoscope, accessories, narrow band spectrum devices →

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