Kangaroo 763662Recalls & reported problems
Cardinal Health, Inc. · Joey Pump Set with Flush Bag,Anti-free Flow · Class 2
All models of Kangaroo (145)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 11
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 11 adverse event reports that list this exact device (DI 10884521072312), received between Jun 13, 2017 and Oct 23, 2023 — classified as 11 malfunctions.
The most frequently reported specific device problem is “Fluid/Blood Leak” (8 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. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.
Reports received per month
Most reported problems
Device problems
- Fluid/Blood Leak8
- Leak/Splash2
- Air/Gas in Device1
- Crack1
- Material Deformation1
- Obstruction of Flow1
Patient problems
- No Consequences Or Impact To Patient5
- No Clinical Signs, Symptoms or Conditions2
- No Known Impact Or Consequence To Patient2
- Discomfort1
- Weight Changes1
Recent adverse event reports
The 11 most recent of 11 reports, in the reporter's own words as published by the FDA.
MalfunctionOct 23, 2023Air/Gas in Device; Air/Gas in Device
THE CUSTOMER REPORTED THERE WAS AIR PUSHING INTO THE TUBE DURING PATIENT USE WITH LEAKAGE FROM THE FORMULA BUT NO ADVERSE EFFECT FROM THE PATIENT. PER ADDITIONAL INFORMATION PROVIDED ON (B)(6) 2023, THE FORMULA APPEARED TO BE COMING OUT OF SOMEWHERE IN THE TUBING ATTACHMENTS INSIDE THE PUMP, SHE BELIEVES IT WAS FROM THE VALVE AND THE FORMULA WENT INSIDE THE DIGITAL DISPLAY OF THE PUMP AT ONE POINT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17984684 ↗MalfunctionApr 22, 2021Fluid/Blood Leak; Obstruction of Flow; Fluid/Blood Leak; Obstruction of Flow
THE CUSTOMER REPORTED THAT AT APPROXIMATELY 4:30 THE PUMP WAS STARTED PER USUAL FOR A FEEDING. THE DISTAL LINE WAS OCCLUDED, RESULTING IN A SPILLAGE OF FORMULA. THIS IS NOT A FIRST-TIME OCCURRENCE, IT HAPPENS ALL THE TIME IF THE DISTAL END IS OCCLUDED BY CLAMPING. WHEN TESTED IN A TEST ENVIRONMENT IT OCCURS AT LEAST 75% OF THE TIME. ADDITIONAL INFORMATION RECEIVED STATED THE LEAKING OCCURRED AT THE DISTAL TIP OF THE FEEDING SET.
Patient problems: Discomfort
MAUDE report 11710406 ↗MalfunctionFeb 23, 2021Fluid/Blood Leak; Fluid/Blood Leak
THE END USER REPORTED THAT AFTER POURING A CARTON OF RESOURCE INTO THE BAG, THE LIQUID STARTED LEAKING FROM THE TUBE AT THE TOP. SHE CANNOT SAY EXACTLY WHERE THE LEAK CAME FROM. SHE THEN EMPTIED, WASHED, AND SAVED THE BAG. THERE WAS NO PATIENT INJURY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 11365534 ↗MalfunctionAug 11, 2020Fluid/Blood Leak; Fluid/Blood Leak
THE CUSTOMER REPORTED THAT THE JOEY FEED AND FLUSH SPIKE SET LEAKED AT THE SPIKE JUNCTION. THERE WAS NO PATIENT INJURY.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 10391774 ↗MalfunctionJun 2, 2020Fluid/Blood Leak; Fluid/Blood Leak
THE CUSTOMER REPORTED THAT THE DEVICE CRACKED AT THE PORT CAUSING THE NUTRITION TO LEAK. THERE WAS NO PATIENT INJURY.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 10108999 ↗MalfunctionFeb 19, 2020Fluid/Blood Leak; Material Deformation; Fluid/Blood Leak; Material Deformation
THE CUSTOMER STATED THE TUBING WAS MELTED TO ITSELF AND WHEN SHE TRIED TO SEPARATE IT, THE TUBING LEAKED. THERE WAS NO HARM TO THE PATIENT.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 9728069 ↗MalfunctionOct 7, 2019Crack; Fluid/Blood Leak; Crack; Fluid/Blood Leak
THE CUSTOMER REPORTED THAT THE FEEDING BAG HAD MANY SLITS AND THERE WERE LEAKS NEAR THE TUBING. THE FEED FLOWED FREELY OUT OF THE BAG AND ONTO THE FLOOR.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 9161546 ↗MalfunctionSep 12, 2019Fluid/Blood Leak; Fluid/Blood Leak
THE CUSTOMER REPORTED THAT THERE WAS A LEAK AT THE CONNECTOR AT THE BOTTOM OF THE BAG.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 9006509 ↗MalfunctionJul 5, 2019Fluid/Blood Leak; Fluid/Blood Leak
THE CUSTOMER REPORTED THAT THE BAG IS LEAKING AT THE SEAM. THERE WAS NO HARM TO THE PATIENT.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 8764472 ↗MalfunctionJul 3, 2018Leak/Splash; Leak/Splash
THE CUSTOMER REPORTED THAT THE ENTERAL FEEDING SETS ARE LEAKING AND CAUSING THE PATIENT TO LOSE WEIGHT. UPON FOLLOW UP THE CUSTOMER STATED THAT THE PATIENT IS USING A JOEY FEEDING PUMP WITH KATE FARMS FORMULA AND THE SETS WERE LEAKING AT DIFFERENT LOCATIONS, SOMETIMES 2-3" UNDER THE BAG OR IN THE MIDDLE OF THE TUBING, ETC. THE PATIENT HAS LOST 15LBS IN A WEEK IN A HALF. NO MEDICAL INTERVENTION HAS BEEN REQUIRED. THE CUSTOMER STATED SHE WAS GOING TO CALL THE PATIENT'S DOCTOR TO DOCUMENT THE WEIGHT LOSS.
Patient problems: Weight Changes
MAUDE report 7660188 ↗MalfunctionJun 13, 2017Leak/Splash; Leak/Splash
ACCORDING TO THE REPORTER, THE CUSTOMER NOTICED THAT THE FEED/FLUSH SET WAS LEAKING ENTERAL FEED OVER THE PUMP THERE WAS MULTIPLE FLOW ERROR ALARMS WHICH WERE RESET WITHOUT INTERVENTION.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 6636872 ↗
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 and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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