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Kangaroo 60EYRecalls & reported problems

Cardinal Health, Inc. · Bifurcated Extension Set · Class 2

Adverse event reports
2
Deaths reported
0
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 20884521143934), received between May 28, 2019 and Jun 6, 2019 — classified as 2 malfunctions.

The most frequently reported specific device problem is “Fluid/Blood Leak” (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. How this data works · Data updated Oct 13, 2026.

Most reported problems

Device problems

  • Fluid/Blood Leak1
  • Fracture1

Patient problems

  • No Consequences Or Impact To Patient1
  • No Patient Involvement1

Recent adverse event reports

The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

  • MalfunctionJun 6, 2019Fluid/Blood Leak; Fluid/Blood Leak

    THE CUSTOMER REPORTS THAT THE NURSE CLAMPED PORT APPROPRIATELY. MILK NOTED TO BE COMING OUT OF THE AREA WHERE TUBING MEETS ¿CHRISTMAS TREE¿ PART OF TUBING. THEY INSPECTED TUBING AND FOUND A SMALL LEAK IN EXTENSION TUBING SET. CONTINUOUS FEED HAD TO BE STOPPED AND EXTENSION SET HAD TO BE REPLACED.

    Patient problems: No Consequences Or Impact To Patient

    MAUDE report 8676723 ↗
  • MalfunctionMay 28, 2019Fracture; Fracture

    THE CUSTOMER REPORTS THAT THE PACKAGE WAS OPENED, AND THE TUBE WAS FOUND TO BE CUT THROUGH.

    Patient problems: No Patient Involvement

    MAUDE report 8647399 ↗

Other TUBES, GASTROINTESTINAL (AND ACCESSORIES) devices

All TUBES, GASTROINTESTINAL (AND ACCESSORIES) devices →

Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.