Skip to content

DISPOSABLE ELECTROSURGICAL SNARE SD-221U-25 (REF N4470530)Recalls & reported problems

Olympus Medical Systems Corp. · Class 2

All models of DISPOSABLE ELECTROSURGICAL SNARE (13)

Data updated Oct 18, 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 04953170326370), received between Jun 20, 2023 and Jun 20, 2023 — classified as 1 malfunction.

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

Most reported problems

Device problems

  • Detachment of Device or Device Component1

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.

  • MalfunctionJun 20, 2023Detachment of Device or Device Component; Detachment of Device or Device Component

    THE CUSTOMER REPORTED TO OLYMPUS, THE DISPOSABLE ELECTROSURGICAL SNARE LOOP AUTOMATICALLY FELL OFF, AFTER CLEANING THE ITEM A SUCTION DEVICE WAS USED TO REMOVE THE POLYP. THE ISSUE WAS FOUND DURING A THERAPEUTIC POLYPECTOMY PROCEDURE, THE PROCEDURE WAS COMPLETED WITH THE SAME DEVICE WITH A 2 ¿ 3 MINUTE DELAY. THERE WERE NO REPORTS OF PATIENT HARM.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 17163749 ↗

Other Gastroscope And Accessories, Flexible/Rigid devices

All Gastroscope And Accessories, Flexible/Rigid devices →

Sources and updates

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