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Kangaroo 674669Recalls & reported problems

Cardinal Health, Inc. · ePump Proximal Spike Set With Flush Bag · Class 2

Adverse event reports
1
Deaths reported
0
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10884521028258), received between Aug 3, 2017 and Aug 3, 2017 — classified as 1 malfunction.

The most frequently reported specific device problem is “Detachment Of Device Component” (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

  • Detachment Of Device Component1
  • Leak/Splash1

Patient problems

  • No Known Impact Or Consequence To Patient1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • MalfunctionAug 3, 2017Detachment Of Device Component; Leak/Splash; Detachment Of Device Component; Leak/Splash

    ACCORDING TO THE REPORTER DURING USE THE ENTERAL FEEDING SET'S TUBING DISCONNECTED FROM THE ADAPTER CAUSING LEAKAGE.

    Patient problems: No Known Impact Or Consequence To Patient

    MAUDE report 6764067 ↗

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.