Kangaroo B5FDRecalls & reported problems
Cardinal Health 200, LLC · Kangaroo Omni Feeding Set, For use with ENfit Connection System, 500 mL. · 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 10885380177125), received between Feb 6, 2025 and Jan 13, 2026 — classified as 3 malfunctions.
The most frequently reported specific device problem is “Air/Gas in Device” (3 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. How this data works · Data updated Oct 13, 2026.
Reports received per month
Most reported problems
Device problems
- Air/Gas in Device3
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.
MalfunctionJan 13, 2026Air/Gas in Device
THE CUSTOMER REPORTED BUBBLES WERE OBSERVED IN THE SET DURING FEEDING.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24052909 ↗MalfunctionMar 7, 2025Air/Gas in Device; Air/Gas in Device
THE CUSTOMER REPORTED THEY WERE USING THE KANGAROO BAG (FOR THE KANGAROO PUMP) TO SET UP A FEED FOR A PATIENT. WHEN THEY PRIMED THE BAG, AIR WAS NOTICED IN THE LINE AND THEY FOUND THE BAG TO BE LEAKING. THEY NOTICED A CUT IN THE TUBING THAT WAS CONTRIBUTING TO THE LEAKING. THEY TRIED TO TAPE THE CUT TO SEE IF THE FEED COULD STILL RUN, BUT THE LEAK PERSISTED. THEY TRANSFERRED THE MILK TO A NEW KANGAROO BAG THAT WAS NOT LEAKING AND PUT THE OTHER ONE TO THE SIDE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21546571 ↗MalfunctionFeb 6, 2025Air/Gas in Device; Air/Gas in Device
THE CUSTOMER REPORTED THE PUMP IS PULLING AIR THROUGH INSTEAD OF MILK. BIOMED FOUND WHEN THEY HOOKED UP THE CASSETTE, AS SOON AS THE PUMP STARTED AND IT TRIED TO LOCK THE CASSETTE ON, IT PUSHED THE CASSETTE AWAY MAKING IT SIT AT A WEIRD ANGLE. THE CASSETTE SEEMS TO HAVE A BIT OF DEFORMITY ON THE INNER PLASTIC PART. THEY FOUND THE ISSUE SEEMED TO BE THE COMBINATION OF THE AFFECTED CASSETTE AND THE PUMP. THE CASSETTE ON A DIFFERENT PUMP DOES NOT HAVE THE ISSUE, AND THE PUMP WITH A NEW CASSETTE DOES NOT HAVE THE ISSUE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21322419 ↗
Other Pump, infusion, enteral devices
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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: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.