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CONNECTING TUBE MAJ-1515 (REF N2645900)Recalls & reported problems

Olympus Medical Systems Corp. · Class 2

All models of CONNECTING TUBE (23)

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 04953170234040), received between Jun 2, 2021 and Jun 2, 2021 — classified as 1 malfunction.

The most frequently reported specific device problem is “Separation 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 18, 2026.

Most reported problems

Device problems

  • Separation 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.

  • MalfunctionJun 2, 2021Separation Problem; Separation Problem

    OLYMPUS MEDICAL SYSTEMS CORP. (OMSC) WAS INFORMED THAT DURING THE REPROCESSING USING OER-5, THE CONNECTION ON THE SCOPE SIDE BECAME LOOSE AND THE TUBE CAME OFF THE SCOPE. THERE WAS NO REPORT OF PATIENT INJURY ASSOCIATED WITH THE EVENT.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 11925810 ↗

Other ACCESSORIES, CLEANING, FOR ENDOSCOPE devices

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Sources and updates

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