Skip to content

Olympus A22205BRecalls & reported problems

OLYMPUS Winter & Ibe GmbH · HF-resection electrode, loop, · 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 04042761021371), received between Feb 14, 2023 and Feb 14, 2023 — classified as 1 malfunction.

The most frequently reported specific device problem is “Material Split, Cut or Torn” (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

  • Material Split, Cut or Torn1

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.

  • MalfunctionFeb 14, 2023Material Split, Cut or Torn; Material Split, Cut or Torn

    OLYMPUS (OMSC) WAS INFORMED, AT THE TIME OF UNPACKAGING THE MEDICAL STAFF CONDUCTED A PREPARATION FOR USE INSPECTION AND FOUND THAT THE ELECTRODE PART HAD BEEN CUT (NO DROPOUTS). THE PROCEDURE WAS COMPLETED USING ANOTHER DEVICE. NO DEATH OR INJURY AND NO IMPACT TO PATIENT WAS REPORTED TO OLYMPUS.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 16369821 ↗

Other Hysteroscope (And Accessories) devices

All Hysteroscope (And Accessories) devices →

Sources and updates

How reports and recalls are matched · Editorial policy · Report an error on this page