Kangaroo 60ENS (UDI 10192253023152)Recalls & reported problems
Cardinal Health 200, LLC · Kangaroo 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 10192253023152), received between Nov 20, 2024 and Dec 30, 2024 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Break” (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.
Reports received per month
Most reported problems
Device problems
- Break1
- Material Separation1
Patient problems
- No Clinical Signs, Symptoms or Conditions2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionDec 30, 2024Break; Break
THE CUSTOMER REPORTED THAT THE NURSE WAS GETTING A FEEDING READY TO ADMINISTER AND OPENED THE KANGAROO EXTENSION SET STOCKED AT BEDSIDE TO FIND IT BROKEN IN PIECES.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21036856 ↗MalfunctionNov 20, 2024Material Separation; Material Separation
THE CUSTOMER REPORTED THE ITEM WAS FOUND IN THE PACKAGE SLICED IN HALF.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20736877 ↗
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.