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Kangaroo 8884711550Recalls & reported problems

Cardinal Health, Inc. · Feeding Tube,Dual Port with Radiopaque Line, Non-weighted · 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 10884521009707), received between Oct 1, 2020 and Oct 13, 2020 — classified as 2 malfunctions.

The most frequently reported specific device problem is “Obstruction of Flow” (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

  • Obstruction of Flow2

Patient problems

  • No Consequences Or Impact To Patient2

Recent adverse event reports

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

  • MalfunctionOct 13, 2020Obstruction of Flow; Obstruction of Flow

    THE CUSTOMER REPORTED THAT THEY WERE ABLE TO GIVE FLUID THROUGH THE FEEDING TUBE VIA A DALE ACE CONNECTOR WHEN THE TUBING END WAS PLACED IN A SINK BUT WHEN TRYING TO DO THIS ON THE PATIENT'S TUBE, THEY WERE NOT ABLE TO FLUSH THE TUBING. THE HAVE TRIED SEVERAL ACE CONNECTORS FROM THEIR STOCK AND ALL WORKED FINE LEADING THEM TO BELIEVE THAT THERE IS AN ISSUE WITH THE TUBE. THERE WAS NO PATIENT INJURY. ADDITIONAL INFORMATION PROVIDED BY THE CUSTOMER STATED THAT THE NURSES ENDED UP USING DECLOGGING MEDICATION (CREON) WHICH WORKED. THE PATIENT'S TUBE WAS REMOVED ON (B)(6) 2020. THERE HAD NOT BEEN ANY MEDS PUT DOWN THE TUBE WHEN THE ISSUE OCCURRED. THE PATIENT HAD THE TUBE FOR MEDS ONLY BUT HAD NOT YET HAD ANY. THE STYLET WAS OUT OF THE TUBE WHEN THE ISSUE OCCURRED.

    Patient problems: No Consequences Or Impact To Patient

    MAUDE report 10675014 ↗
  • MalfunctionOct 1, 2020Obstruction of Flow; Obstruction of Flow

    THE CUSTOMER REPORTED THAT THEY WERE ABLE TO GIVE FLUID THROUGH THE FEEDING TUBE VIA A DALE ACE CONNECTOR WHEN THE TUBING END WAS PLACED IN A SINK BUT WHEN TRYING TO DO THIS ON THE PATIENT'S TUBE, THEY WERE NOT ABLE TO FLUSH THE TUBING. THE HAVE TRIED SEVERAL ACE CONNECTORS FROM THEIR STOCK AND ALL WORKED FINE LEADING THEM TO BELIEVE THAT THERE IS AN ISSUE WITH THE TUBE. THERE WAS NO PATIENT INJURY.

    Patient problems: No Consequences Or Impact To Patient

    MAUDE report 10617352 ↗

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Sources and updates

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