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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

Nov 2023: 0 reportsDec 2023: 0 reportsJan 2024: 0 reportsFeb 2024: 0 reportsMar 2024: 0 reportsApr 2024: 0 reportsMay 2024: 0 reportsJun 2024: 0 reportsJul 2024: 0 reportsAug 2024: 0 reportsSep 2024: 0 reportsOct 2024: 0 reportsNov 2024: 0 reportsDec 2024: 0 reportsJan 2025: 0 reportsFeb 2025: 0 reportsMar 2025: 0 reportsApr 2025: 0 reportsMay 2025: 0 reportsJun 2025: 0 reportsJul 2025: 0 reportsAug 2025: 0 reportsSep 2025: 0 reportsOct 2025: 0 reportsNov 2025: 0 reportsDec 2025: 0 reportsJan 2026: 0 reportsFeb 2026: 0 reportsMar 2026: 0 reportsApr 2026: 0 reportsMay 2026: 0 reportsJun 2026: 0 reportsJul 2026: 0 reportsAug 2026: 0 reportsSep 2026: 0 reportsOct 2026: 0 reports2024202520261
Last 36 months. The most recent month may be incomplete.

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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Sources and updates

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