Kangaroo BSPFFRecalls & reported problems
Cardinal Health 200, LLC · Kangaroo Omni Feeding Set with Flush Bag 1000mL and ENPlus Spike · Class 2
Data updated Oct 13, 2026 from official FDA records · Editorial policy
- 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 10885380177156), received between Oct 9, 2024 and Mar 31, 2025 — 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.
MalfunctionMar 31, 2025Air/Gas in Device; Air/Gas in Device
THE CUSTOMER REPORTED THEY RAN A MANUAL TEST USING A BSPFF SET, AND THE PUMP PASSED THE TESTING. THEY TRIED RUNNING A FLUSH NOW, AND INITIALLY GOT A FLUSH ERROR, THEN THEY OBSERVED AIR IN THE FLUSH TUBE. FORMULA USED WAS NESTLE FIBERSOURCE READY TO HANG.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21730386 ↗MalfunctionMar 25, 2025Air/Gas in Device; Air/Gas in Device
THE CUSTOMER REPORTED THE PUMP SEEMS OVERLY SENSITIVE TO EVEN SMALL BUBBLES IN THE TUBING BEFORE THE CARTRIDGE, CAUSING THE PUMP TO STOP FEEDING. THIS CAN BE PROBLEMATIC AS IT DISRUPTS THE CONTINUOUS FEEDING PROCESS.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21686883 ↗MalfunctionOct 9, 2024Air/Gas in Device; Air/Gas in Device
THE CUSTOMER REPORTED THE PUMP WAS ALARMING AND THERE WERE A LOT OF FINE BUBBLES IN THE TUBING BETWEEN THE FEED SPIKE AND THE PUMP. THE PUMP ALARMED IMMEDIATELY AFTER BEING CONNECTED, SAYING THERE WAS A PROBLEM BETWEEN THE BAG AND THE PUMP. THEY REMOVED THE SET AND GOT ANOTHER SET.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20406614 ↗
Other Pump, infusion, enteral devices
- Kangaroo 775100Cardinal Health, Inc. · PUMP, INFUSION, ENTERAL988 reports
- 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.
How reports and recalls are matched · Editorial policy · Report an error on this page