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Kangaroo 77500FDRecalls & reported problems

Cardinal Health, Inc. · Connect Feeding Set,Anti-free Flow · Class 2

Adverse event reports
13
Deaths reported
0
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 13 adverse event reports that list this exact device (DI 10884521190849), received between Dec 9, 2019 and Dec 17, 2020 — classified as 13 malfunctions.

The most frequently reported specific device problem is “Fluid/Blood Leak” (13 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

  • Fluid/Blood Leak13

Patient problems

  • No Consequences Or Impact To Patient8
  • No Patient Involvement3
  • Hypoglycemia1
  • No Clinical Signs, Symptoms or Conditions1

Recent adverse event reports

The 13 most recent of 13 reports, in the reporter's own words as published by the FDA.

  • MalfunctionDec 17, 2020Fluid/Blood Leak; Fluid/Blood Leak

    THE CUSTOMER REPORTED THAT THE END USER EXPERIENCED PUMP SET TUBING COMING APART AT THE CASSETTE, ESPECIALLY WHEN PRIMING. ADDITIONAL INFORMATION RECEIVED FROM THE CUSTOMER STATED THAT THERE WAS A LEAK AS THE TUBING WAS DISCONNECTED. THERE WAS NO PATIENT HARM REPORTED.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 11030494 ↗
  • MalfunctionDec 4, 2020Fluid/Blood Leak; Fluid/Blood Leak

    THE CUSTOMER REPORTED THAT THE LOAD SET WAS LEAKING UPON USE PER VISUAL. THERE WAS NO PATIENT HARM.

    Patient problems: No Consequences Or Impact To Patient

    MAUDE report 10945482 ↗
  • MalfunctionAug 13, 2020Fluid/Blood Leak; Fluid/Blood Leak

    THE CUSTOMER REPORTED THAT THE TUBING GOING INTO THE CASSETTE OF THE CONNECT PUMP SET GOT DISCONNECTED AND LEAKED ALL OVER INCLUDING THE PUMP. THERE WAS NO PATIENT HARM REPORTED.

    Patient problems: No Consequences Or Impact To Patient

    MAUDE report 10401237 ↗
  • MalfunctionJul 10, 2020Fluid/Blood Leak; Fluid/Blood Leak

    THE CUSTOMER REPORTED THAT THE CASSETTE WAS LEAKING.

    Patient problems: No Consequences Or Impact To Patient

    MAUDE report 10257707 ↗
  • MalfunctionJul 9, 2020Fluid/Blood Leak; Fluid/Blood Leak

    THE CUSTOMER REPORTED THE CASSETTE WAS LEAKING. THERE WAS NO HARM TO THE PATIENT.

    Patient problems: No Consequences Or Impact To Patient

    MAUDE report 10251151 ↗
  • MalfunctionJul 8, 2020Fluid/Blood Leak; Fluid/Blood Leak

    THE CUSTOMER STATES THEIR DAUGHTER USES THE KANGAROO CONNECT PUMP WITH THE 500 ML BAGS FOR FEEDING WITH HER NASOGASTRIC (NG) TUBE. OVER THE PAST FEW WEEKS, SEVERAL BAGS WERE LEAKING AT THE JUNCTION WHERE THE TUBE ENTERS AND EXITS THE CASSETTE.

    Patient problems: No Consequences Or Impact To Patient

    MAUDE report 10246028 ↗
  • MalfunctionFeb 21, 2020Fluid/Blood Leak; Fluid/Blood Leak

    THE CUSTOMER REPORTED THAT FORMULA HAD BEEN POURED INTO THE BAG AND WAS INTACT. THE BAG WAS THEN PLACED IN THE FRIDGE FOR SEVERAL HOURS AND NOTED TO BE LEAKING FORMULA FROM THE BOTTOM OF THE POUCH. THE TUBING WAS NOT INVOLVED. THE STAFF ESTIMATED THAT THIS WAS THE FIRST DAY OF BAG USE BUT WAS UNSURE IF PREVIOUS FEED HAD BEEN DELIVERED.

    Patient problems: No Consequences Or Impact To Patient

    MAUDE report 9739953 ↗
  • MalfunctionFeb 20, 2020Fluid/Blood Leak; Fluid/Blood Leak

    THE CUSTOMER REPORTED THAT THE KANGAROO CONNECT 500ML FEEDING BAG WAS LEAKING INSIDE THE CASSETTE AT THE CONNECTION WHERE THE HARD PLASTIC WHITE PIECE MEETS THE TUBING INSIDE OF THE CASSETTE, RIGHT BESIDE WHERE THE SMALL BLACK CIRCULAR PIECE IS WITHIN THE CASSETTE. THE FORMULA BEING USED WAS NEOCATE. THERE ARE NO OTHER DETAILS AVAILABLE.

    Patient problems: No Consequences Or Impact To Patient

    MAUDE report 9734503 ↗
  • MalfunctionFeb 11, 2020Fluid/Blood Leak; Fluid/Blood Leak

    THE CUSTOMER REPORTED THAT A CHILD WAS RECEIVING FEED VIA A KANGAROO CONNECT PUMP OVERNIGHT AND AT APPROXIMATELY 0400H STAFF NOTED THAT THE FEED HAD LEAKED INTO THE BED. THE STAFF MEMBER WAS UNABLE TO MEASURE THE LOSS OF FEED BUT NOTED THE BG TO BE LOW. THE CHILD IS IDDM AND REQUIRED A SYRUP BOLUS AS RESCUE MEDICATION FOR HYPOGLYCEMIA. THE STAFF ESTIMATED THAT THIS OCCURRED ON THE THIRD DAY OF USE. THERE WAS NO OTHER MEDICAL INTERVENTION PROVIDED BEYOND THE SYRUP BOLUS. THE PATIENT RESPONDED WELL TO THE SYRUP BOLUS AND THEIR SYMPTOMS RESOLVED. THERE ARE NO KNOWN FURTHER COMPLICATIONS AT THIS TIME.

    Patient problems: Hypoglycemia

    MAUDE report 9695615 ↗
  • MalfunctionJan 14, 2020Fluid/Blood Leak; Fluid/Blood Leak

    THE CUSTOMER REPORTED THAT THE FEEDING SET WAS LEAKING FROM THE CASSETTE AS WELL AS FROM THE TOP OF THE BAG. THERE WAS NO PATIENT HARM REPORTED.

    Patient problems: No Consequences Or Impact To Patient

    MAUDE report 9586131 ↗
  • MalfunctionDec 9, 2019Fluid/Blood Leak; Fluid/Blood Leak

    THE CUSTOMER REPORTED LEAKING FROM THE TUBING FOR THE ENTERAL FEEDING SET BEFORE IN-USE ON PATIENT.

    Patient problems: No Patient Involvement

    MAUDE report 9439600 ↗
  • MalfunctionDec 9, 2019Fluid/Blood Leak; Fluid/Blood Leak

    THE CUSTOMER REPORTED LEAKING FROM THE TUBING FOR THE ENTERAL FEEDING SET BEFORE IN-USE ON PATIENT.

    Patient problems: No Patient Involvement

    MAUDE report 9439586 ↗
  • MalfunctionDec 9, 2019Fluid/Blood Leak; Fluid/Blood Leak

    THE CUSTOMER REPORTED LEAKING FROM THE TUBING FOR THE ENTERAL FEEDING SET BEFORE IN-USE ON PATIENT.

    Patient problems: No Patient Involvement

    MAUDE report 9439585 ↗

Other PUMP, INFUSION, ENTERAL devices

All PUMP, INFUSION, ENTERAL devices →

Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.