Kangaroo 8884705008Recalls & reported problems
Cardinal Health, Inc. · Y-Site Extension · Class 2
All models of Kangaroo (145)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- 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 10884521000063), received between May 11, 2023 and Jul 24, 2023 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Fluid/Blood Leak” (2 reports).
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
- Fluid/Blood Leak2
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.
MalfunctionJul 24, 2023Fluid/Blood Leak; Fluid/Blood Leak
THE CUSTOMER REPORTED THE KANGAROO EXTENSION TUBE WAS ADDED PRIOR TO THE TUBE FEED. FEEDS RUN OVER 90 MINS. SIXTY MINUTES INTO THE FEED, THE NURSE NOTICED THE FEED LEAKED ONTO THE MATTRESS. THE MED PORT ON THE EXTENSION TUBE OPENED UP TOO EASILY, EVEN THOUGH IT WAS CLOSED PRIOR TO FEED INITIATION. THERE WAS NO PATIENT HARM.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17378032 ↗MalfunctionMay 11, 2023Fluid/Blood Leak; Fluid/Blood Leak
THE CUSTOMER REPORTED THAT THE PATIENT WAS FOUND IN BED LAYING IN LEAKED TUBE FEED. THE FEED WAS NOTED TO BE IN A PUDDLE ON THE FLOOR AND COVERING THE BED AND PATIENT. ON INSPECTION OF THE LINE, THE MAIN PORT WAS OPEN AND THE TUBE FEED LINE WAS CONNECTED TO Y SITE PORT. AS FOR THE DEVICE, THEY BELIEVE THERE IS A PROBLEM WHEN THE FEED LINE IS PUT INTO THE SECONDARY PORT TO RUN. THEY FIND THAT IT CAUSES THE MAIN PORT TO POP OPEN FROM PRESSURE. WHEN THE FEED LINE IS IN THE MAIN PORT, THE Y SITE OR SECONDARY PORT DOES NOT OPEN. IF THE FEED LINE WILL NO LONGER STAY IN THE MAIN PORT THEN THEY SHOULD BE CHANGING THE EXTENSION TUBE. THE IMPACT OF THE INCIDENT WAS THAT THE PATIENT MISSED A FEED AND REQUIRED A THOROUGH BED BATH. THE PATIENT IS AT RISK FOR SKIN BREAK DOWN BUT NO INJURIES WERE REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16912354 ↗
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Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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