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Kangaroo 776150Recalls & reported problems

Cardinal Health, Inc. · Epump and Joey Burette Recertification Set · Class 2

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 10884521022126), received between May 10, 2017 and May 13, 2021 — classified as 2 malfunctions.

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

  • Fluid/Blood Leak1
  • Leak/Splash1

Patient problems

  • No Clinical Signs, Symptoms or Conditions1
  • No Patient Involvement1

Recent adverse event reports

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

  • MalfunctionMay 13, 2021Fluid/Blood Leak; Fluid/Blood Leak

    THE CUSTOMER REPORTED THAT THE RECERTIFICATION SETS ARE LEAKING AND CAUSING ALL RECERTIFICATIONS TO FAIL. ADDITIONAL INFORMATION RECEIVED STATED THAT THE LEAK WAS AROUND THE PLASTIC TAB ON THE SET, ALMOST LIKE A PUSH POINT ON THE SET. THIS OCCURRED DURING TESTING. NO PATIENT INVOLVEMENT.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 11817038 ↗
  • MalfunctionMay 10, 2017Leak/Splash; Leak/Splash

    THE INITIAL REPORTER STATES THE FEEDING SETS ARE LEAKING FROM THE VALVE TOWARDS THE FILLING CHAMBER.

    Patient problems: No Patient Involvement

    MAUDE report 6556898 ↗

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.