Kangaroo 8884705008E (UDI 10192253011135)Recalls & reported problems
Cardinal Health 200, LLC · Y-Site Extension with ENFit Connection · Class 2
All models of Kangaroo (35)
Data updated Oct 16, 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 10192253011135), received between Apr 1, 2026 and Apr 16, 2026 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Break” (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 16, 2026.
Reports received per month
Most reported problems
Device problems
- Break2
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.
MalfunctionApr 16, 2026Break
THE CUSTOMER REPORTED A NURSE HAD AN ISSUE WHILE SETTING UP A REFEED OF INFUSION FOR A PATIENT. THE CONNECTOR TUBING BROKE AT THE Y-CONNECTION SITE WHILE THE NURSE WAS TRYING TO CONNECT IT TO THE PATIENT. THE NURSE WAS ABLE TO GET ANOTHER SET OF TUBING TO USE FOR THE REFEED. THERE WAS VERY LITTLE OF THE REFEED LOST DUE TO THE BROKEN SET. THERE WAS NO HARM TO THE PATIENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24903202 ↗MalfunctionApr 1, 2026Break
THE CUSTOMER REPORTED THE MIDDLE OF ONE OF THE PORTS ON THE EXTENSION FOR THE G-TUBE BROKE OFF. THE CUSTOMER WAS NOT ABLE TO CLOSE THE PORT WHEN IT WAS NOT IN USE. IT POSSIBLY BROKE OFF DUE TO ATTACHING TO THE PORT TOO TIGHTLY, BUT THEY HAVE NEVER SEEN ONE BREAK OFF AT THAT SPOT BEFORE. NO HARM WAS DONE TO THE PATIENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24752980 ↗
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- Kangaroo 382400Cardinal Health, Inc. · PUMP, INFUSION, ENTERAL677 reports
- Kangaroo 383400Cardinal Health, Inc. · Pump, Infusion, Enteral1 death659 reports
- Infinity Enteral Feeding Pump INFKIT2Zevex International, Inc. · Pump, Infusion, Enteral2 deaths407 reports
- Infinity Enteral Feeding Pump INFP01Zevex International, Inc. · Pump, Infusion, Enteral1 death207 reports
- Perfusor® 8713030UB. Braun Medical Inc. · Pump, infusion, enteral2 recalls3 deaths76 reports
- Kangaroo 775659Cardinal Health, Inc. · PUMP, INFUSION, ENTERAL1 death139 reports
- Perfusor® 8713031UB. Braun Medical Inc. · PUMP, INFUSION, ENTERAL1 recall21 deaths87 reports
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 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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