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NA 242271Recalls & reported problems

Medos International Sàrl · HD C-Mount Arthroscope/Sinuscope compatible with Mitek lock 3.5 mm x 30 deg x 205 mm · Class 2

Data updated Oct 16, 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 10886705032099), received between Apr 18, 2022 and Apr 18, 2022 — classified as 1 malfunction.

The most frequently reported specific device problem is “Display or Visual Feedback Problem” (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 16, 2026.

Most reported problems

Device problems

  • Display or Visual Feedback Problem1

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.

  • MalfunctionApr 18, 2022Display or Visual Feedback Problem; Display or Visual Feedback Problem

    IT WAS REPORTED THROUGH IN-HOUSE DISTRIBUTION THAT THE C-MOUNT ENDOSCOPE, 30 DEGREE, 3.5 MM X 205 MM, MITEK LOCK DEVICE HAD A FOGGY IMAGE. THERE WAS NO PROCEDURE NOR PATIENT INVOLVEMENT REPORTED. NO ADDITIONAL INFORMATION WAS PROVIDED.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 14134979 ↗

Other Nasopharyngoscope (flexible or rigid) devices

All Nasopharyngoscope (flexible or rigid) devices →

Sources and updates

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