Kangaroo 382401Recalls & reported problems
Cardinal Health, Inc. · Epump Enteral Feed and Flush Pump with Pole Clamp,Programmable,Refurbished · Class 2
- Adverse event reports
- 18
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 18 adverse event reports that list this exact device (DI 10884521006621), received between Jun 28, 2017 and Jun 26, 2021 — classified as 18 malfunctions.
The most frequently reported specific device problem is “Excess Flow or Over-Infusion” (11 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.
Most reported problems
Device problems
- Excess Flow or Over-Infusion11
- Inaccurate Delivery2
- Inaccurate Flow Rate2
- Appropriate Device Problem Term/Code Not Available1
- Device Stops Intermittently1
- Sparking1
Patient problems
- No Clinical Signs, Symptoms or Conditions15
- No Consequences Or Impact To Patient2
- No Patient Involvement1
Recent adverse event reports
The 18 most recent of 18 reports, in the reporter's own words as published by the FDA.
MalfunctionJun 26, 2021Inaccurate Flow Rate; Inaccurate Flow Rate
THE CUSTOMER REPORTED THAT THE DEVICE WAS RUNNING FASTER.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 12072913 ↗MalfunctionJun 26, 2021Inaccurate Flow Rate; Inaccurate Flow Rate
THE CUSTOMER REPORTED THAT THE RATE WAS BEING DELIVERED HIGHER THAN ACCEPTABLE DEVIATION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 12072908 ↗MalfunctionJun 26, 2021Excess Flow or Over-Infusion; Excess Flow or Over-Infusion
THE CUSTOMER REPORTED AN ISSUE OF TOO MUCH LIQUID.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 12072904 ↗MalfunctionJun 26, 2021Excess Flow or Over-Infusion; Excess Flow or Over-Infusion
THE CUSTOMER REPORTED THAT THE DEVICE HAD OVERFEEDING ISSUE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 12072888 ↗MalfunctionJun 26, 2021Excess Flow or Over-Infusion; Excess Flow or Over-Infusion
THE CUSTOMER REPORTED THAT THE DEVICE WAS OUT OF SPEC AND HAD EXCESS. THERE WERE NO FURTHER INFORMATION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 12072860 ↗MalfunctionJun 26, 2021Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
THE CUSTOMER REPORTED THAT THE DEVICE HAS BURNT CASE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 12072746 ↗MalfunctionJun 25, 2021Excess Flow or Over-Infusion; Excess Flow or Over-Infusion
THE CUSTOMER REPORTED THAT THE DEVICE WAS OUT OF SPEC, IN EXCESS.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 12071411 ↗MalfunctionJun 25, 2021Excess Flow or Over-Infusion; Excess Flow or Over-Infusion
THE CUSTOMER REPORTED THAT THE DEVICE WAS OVER FEEDING.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 12071349 ↗MalfunctionJun 25, 2021Excess Flow or Over-Infusion; Excess Flow or Over-Infusion
THE CUSTOMER REPORTED THAT THE DEVICE HAD AN OUT OF SPEC HIGH.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 12071222 ↗MalfunctionJun 25, 2021Sparking; Sparking
THE CUSTOMER REPORTED THAT THE DEVICE WAS SPARKING.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 12071160 ↗MalfunctionJun 3, 2021Excess Flow or Over-Infusion; Excess Flow or Over-Infusion
THE CUSTOMER REPORTED AN ISSUE OF OVERFEEDING. THERE WAS A FLOW RATE ISSUE WHERE IT WAS 50% HIGHER WHILE DOING PREVENTATIVE MAINTENANCE. ADDITIONAL INFORMATION WAS RECEIVED STATING THAT THE VOLUME ON THIS ASSET WAS SET TO 20ML AT A RATE OF 300ML/HR. THE DEVICE DELIVERED 30MLS.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 11932865 ↗MalfunctionMay 26, 2021Excess Flow or Over-Infusion; Excess Flow or Over-Infusion
THE CUSTOMER REPORTED THAT THE KANGAROO EPUMP WAS NOT GIVING ACCURATE FEED. ADDITIONAL INFORMATION PROVIDED ON 25MAY2021, STATED THAT THE PUMP WAS DELIVERING MORE THAN THE AMOUNT IT SHOULD. THERE WAS NO PATIENT INJURY. NO FURTHER INFORMATION CAN BE PROVIDED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 11890447 ↗MalfunctionMay 24, 2021Inaccurate Delivery; Inaccurate Delivery
THE CUSTOMER REPORTED THAT WHEN THEY ARE TRYING TO RUN 50 MILLILITER, THE PUMP IS DELIVERING 60 MILLILITER INSTEAD. THERE WAS NO PATIENT HARM.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 11872575 ↗MalfunctionApr 22, 2021Excess Flow or Over-Infusion; Excess Flow or Over-Infusion
THE CUSTOMER REPORTED THAT THE DEVICE HAD AN OVERFEEDING ISSUE. ADDITIONAL INFORMATION WAS RECEIVED STATED THAT THE ISSUE OCCURRED DURING TESTING. THE VOLUME TO BE INFUSED WAS SET TO 300ML. THE VOLUME TO BE DELIVERED WAS 10ML. THEY WERE EXPECTING AROUND 10 ML TO BE DELIVERED BUT THE DEVICE DELIVERED OVER 20 ML. THE DEVICE WAS STILL PUMPING SO THEY POWERED IT DOWN. NO FURTHER DETAILS PROVIDED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 11711058 ↗MalfunctionApr 19, 2021Inaccurate Delivery; Inaccurate Delivery
THE CUSTOMER REPORTED THAT THE RATE OF THE DEVICE WAS OUT OF RANGE. DURING PREVENTATIVE MAINTENANCE TESTING, THE VOLUME WAS OVER THE 82.4ML LIMIT WHEN THE DEVICE WAS SET TO CONTINUOUS MODE OF 150ML/HR FOR THE 30MIN ACCURACY TEST.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 11685186 ↗MalfunctionApr 13, 2020Excess Flow or Over-Infusion; Excess Flow or Over-Infusion
THE CUSTOMER REPORTED THAT THE ENTERAL FEEDING PUMP INFUSED MORE THAN WHAT IT WAS PROGRAMMED TO.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 9953615 ↗MalfunctionOct 9, 2019Excess Flow or Over-Infusion; Excess Flow or Over-Infusion
THE CUSTOMER REPORTED THAT WHILE IN USE, THE DEVICE CONTINUED TO RUN AND DID NOT SHUT OFF WHEN THE SET AMOUNT OF FEEDING WAS REACHED. THERE WAS NO HARM TO THE PATIENT.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 9172086 ↗MalfunctionJun 28, 2017Device Stops Intermittently; Device Stops Intermittently
THE CUSTOMER UNIT WAS RETURNED FOR ROUTINE MAINTENANCE. UPON TRIAGE, THE UNIT SHUT OFF AND HAD INTERMITTENT POWER DURING THE RECERTIFICATION TEST. NO PATIENT INJURY REPORTED.
Patient problems: No Patient Involvement
MAUDE report 6672959 ↗
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: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.