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Kangaroo 384400Recalls & reported problems

Cardinal Health, Inc. · Connect Enteral Feeding Pump · Class 2

Data updated Oct 13, 2026 from official FDA records · Editorial policy

Adverse event reports
2
Deaths reported
0
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10884521190894), received between Jan 22, 2020 and Feb 10, 2020 — classified as 2 malfunctions.

The most frequently reported specific device problem is “Excess Flow or Over-Infusion” (1 report).

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-Infusion1
  • Improper Flow or Infusion1

Patient problems

  • No Consequences Or Impact To Patient1
  • No Known Impact Or Consequence To Patient1

Recent adverse event reports

The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

  • MalfunctionFeb 10, 2020Excess Flow or Over-Infusion; Excess Flow or Over-Infusion

    THE CUSTOMER REPORTED THAT WITH A RATE OF 175 ML/HR THE CONNECT FEEDING PUMP FED A 220 ML DOSE IN UNDER A HALF AN HOUR.

    Patient problems: No Consequences Or Impact To Patient

    MAUDE report 9689268 ↗
  • MalfunctionJan 22, 2020Improper Flow or Infusion; Improper Flow or Infusion

    THE CUSTOMER REPORTED THAT THE VOLUME IS ALWAYS NOT PRECISE AND THE UNIT SOMETIMES PUMPS AIR/BUBBLES INTO THE TUBING.

    Patient problems: No Known Impact Or Consequence To Patient

    MAUDE report 9618127 ↗

Other PUMP, INFUSION, ENTERAL devices

All PUMP, INFUSION, ENTERAL devices →

Sources and updates

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