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CARDINAL HEALTH G5VBLRecalls & reported problems

Cardinal Health 200, LLC · Cardinal Health; Dual End 2 - in- 1 Channel/Valve Brush · Class 1

Data updated Oct 18, 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 10885380121456), received between Jul 21, 2017 and Jul 21, 2017 — classified as 1 injury.

The most frequently reported specific device problem is “Detachment Of 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 Component1

Patient problems

  • No Known Impact Or Consequence To Patient1

Recent adverse event reports

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

  • InjuryJul 21, 2017Detachment Of Device Component

    PER THE PHYSICIAN, WHILE IN THE MIDDLE OF AN ESOPHAGOGASTRODUODENOSCOPY, THE BRUSH WITH WIRE FELL OUT OF THE CHANNEL AND LANDED IN THE PATIENT'S STOMACH. THE PHYSICIAN IMMEDIATELY USED FORCEPS TO GRAB THE METAL BRUSH FORCEPS AND USED A ROTH NET TO GRAB THE BRUSH TIP AND PULL THROUGH THE CHANNEL WHILE IN THE STOMACH. THE PHYSICIAN WAS ABLE TO RETRIEVE THE BRUSH.  THE PATIENT SUFFERED NO INJURY AND THE PROCEDURE WAS COMPLETED WITHOUT FURTHER INCIDENT.

    Patient problems: No Known Impact Or Consequence To Patient

    MAUDE report 6731725 ↗

Other ACCESSORIES, CLEANING BRUSHES, FOR ENDOSCOPE devices

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Sources and updates

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