Kangaroo B10FFRecalls & reported problems
Cardinal Health 200, LLC · Kangaroo Omni Feeding Set with Flush Bag 1000mL · Class 2
- 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 10885380177118), received between Jul 29, 2025 and Jul 29, 2025 — 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
- Abdominal Pain1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionJul 29, 2025Air/Gas in Device; Air/Gas in Device
THE CUSTOMER REPORTED THE VALVE IS NOT SEALED PROPERLY AND IS PULLING AIR INTO THE FEEDING SIDE, FILLING THE CONSUMERS STOMACH WITH AIR. THIS IS CAUSING THE PUMP TO GO BACK INTO THE FLUSH MODE, DUE TO AIR BUBBLES IN THE FEED LINE. PUMP FORCES PRIMING BEFORE IT WILL RETURN TO FEED MODE.
Patient problems: Abdominal Pain
MAUDE report 22649445 ↗
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.