Kangaroo 772055 (UDI 10192253009903)Recalls & reported problems
Cardinal Health 200, LLC · Epump Set, Anti-free Flow · Class 2
Data updated Oct 13, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10192253009903), received between Mar 14, 2024 and Mar 14, 2024 — classified as 1 malfunction.
The most frequently reported specific device problem is “Air/Gas in Device” (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
- Air/Gas in Device1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionMar 14, 2024Air/Gas in Device; Air/Gas in Device
THE CUSTOMER STATED THAT WHEN THE PUMP GETS TO 10ML OR 15ML, THE PUMP IS STILL GOING, BUT IT'S PASSING LOTS OF AIR AND CAUSING AIR TO GO INTO THE PATIENT. THE MOTHER TRIED SEVERAL OF THE BAGS AND THE ISSUE CONTINUED TO HAPPEN. THEY ORIGINALLY THOUGHT IT WAS DUE TO THE PUMPS, HOWEVER THEY DIAGNOSED THE PUMPS AND CONFIRMED WITH THEIR TECH THAT IT WAS THE BAGS.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 18903159 ↗
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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 13, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 13, 2026
- Page last rebuilt: Oct 13, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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