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Kangaroo 382400WRecalls & reported problems

Cardinal Health, Inc. · Epump Enteral Feed and Flush Pump with Pole Clamp,Programmable · 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 10884521143876), received between Apr 9, 2021 and May 14, 2021 — classified as 2 malfunctions.

The most frequently reported specific device problem is “Inaccurate Delivery” (2 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

  • Inaccurate Delivery2

Patient problems

  • No Clinical Signs, Symptoms or Conditions2

Recent adverse event reports

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

  • MalfunctionMay 14, 2021Inaccurate Delivery; Inaccurate Delivery

    THE CUSTOMER REPORTED THAT THE DEVICE WAS OVER FEEDING. THERE WAS NO PATIENT INVOLVEMENT. ADDITIONAL INFORMATION WAS RECEIVED STATING THAT THE FEED RATE WAS SET TO 75ML/HR AND AFTER 30 MINUTES IT PUMPED ALMOST 45ML.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 11826257 ↗
  • MalfunctionApr 9, 2021Inaccurate Delivery; Inaccurate Delivery

    THE CUSTOMER REPORTED THAT THE DEVICE WAS FEEDING TOO FAST. ADDITIONAL INFORMATION WAS RECEIVED AND STATED THAT THE PATIENT WAS NOT OVERFED.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 11645266 ↗

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.