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Olympus A22087ARecalls & reported problems

OLYMPUS Winter & Ibe GmbH · Obturator, deflecting tip, 28 Fr. · Class 2

Data updated Oct 13, 2026 from official FDA records · Editorial policy

Adverse event reports
1
Deaths reported
0
Injuries reported
1
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 04042761021203), received between Jun 24, 2021 and Jun 24, 2021 — classified as 1 injury.

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

  • Adverse Event Without Identified Device or Use Problem1

Patient problems

  • Burn(s)1

Recent adverse event reports

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

  • InjuryJun 24, 2021Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

    UPDATE: THE CUSTOMER CLARIFIED 02JUL2021 THAT THE CUSTOMER DOES NOT USE AN OLYMPUS GENERATOR OR OLYMPUS GROUNDING PADS. THE BURN EXPERIENCED BY THE PATIENT IS NOT RELATED TO THE USE OF AN OLYMPUS DEVICE.

    Patient problems: Burn(s)

    MAUDE report 12063808 ↗

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Sources and updates

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