Kangaroo 773656 (UDI 10192253009941)Recalls & reported problems
Cardinal Health 200, LLC · ePUMP SET Anti-free Flow · Class 2
- Adverse event reports
- 3
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 10192253009941), received between Mar 13, 2024 and Sep 15, 2025 — classified as 3 malfunctions.
The most frequently reported specific device problem is “Infusion or Flow Problem” (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
- Infusion or Flow Problem1
Patient problems
- No Clinical Signs, Symptoms or Conditions3
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 15, 2025Infusion or Flow Problem
FEED PUMP ALARMING FOR FEED ERROR DESPITE NO APPARENT KINKS OR CLOGS. FEED BAGS CHANGED MULTIPLE TIMES AC WELL AS FEEDING PUMP AND PROBLEM CONTINUED. LINE WAS FLUSHED AND PRIMED TO CLEAR ANY POTENTIAL CLOGS AS WELL. THE PUMP CONTINUED TO ALARM HOURLY UNTIL CHANGED TO A FEED BAG THAT INCLUDED A FLUSH BAG.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23050591 ↗MalfunctionMar 13, 2024
TUBING BROKE WHILE IN OPERATION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 18893133 ↗MalfunctionMar 13, 2024
TUBING BROKE WHILE IN OPERATION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 18893131 ↗
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.