Skip to content

CONNECTING TUBE MAJ-1904Recalls & 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 04953170299353), received between Jan 30, 2023 and Jan 30, 2023 — classified as 1 malfunction.

The most frequently reported specific device problem is “Device Reprocessing 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

  • Device Reprocessing 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.

  • MalfunctionJan 30, 2023Device Reprocessing Problem; Device Reprocessing Problem

    THE CUSTOMER REPORTED TO OLYMPUS THAT AN UNAPPROVED NEEDLE ATTACHMENT HAD BEEN USED TO REPROCESS THE CONNECTING TUBE. THE ISSUE OCCURRED DURING REPROCESSING, AND THERE WAS NO PATIENT HARM ASSOCIATED WITH THE EVENT.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 16265634 ↗

Other ACCESSORIES, CLEANING, FOR ENDOSCOPE devices

All ACCESSORIES, CLEANING, FOR ENDOSCOPE devices →

Sources and updates

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