Skip to content

Kangaroo 461701ERecalls & reported problems

Cardinal Health, Inc. · Polyurethane Feeding Tube Radiopaque · 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 10884521547162), received between Dec 7, 2021 and Dec 7, 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
  • Material Puncture/Hole1
  • Material Twisted/Bent1

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.

  • MalfunctionDec 7, 2021Material Twisted/Bent; Material Twisted/Bent

    THE CUSTOMER REPORTED THAT A NURSE IN THE NICU FOUND A DEFECTIVE OROGASTRIC (OG) TUBE. PER ADDITIONAL INFORMATION PROVIDED BY THE CUSTOMER, THE NURSE PUSHED AIR INTO THE OG ONCE IT WAS INSERTED TO ENSURE IT WAS IN THE PROPER PLACEMENT AND COULD BE HEARD IN THE STOMACH BUT WAS UNABLE TO HEAR THE AIR. THE RN REMOVED THE OG TUBE FROM THE PATIENT AND ATTEMPTED TO PUSH WATER THROUGH THE OG AT THE SINK AREA. THE WATER PASSED EASILY THROUGH THE TUBE BUT THE BASE OF THE TUBE, THAT WOULD BE IN THE PATIENT'S STOMACH, WAS SLIGHTLY BENT SO THE RN ASSUMED THAT WAS THE ISSUE. THE NURSE DISCARDED AND REPLACED THE FEEDING TUBE WITH NO ISSUES. THERE WAS NO PATIENT HARM AND NO CHANGE IN THE MEDICAL TREATMENT/INTERVENTIONS GIVEN.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 12954490 ↗
  • MalfunctionDec 7, 2021Fluid/Blood Leak; Material Puncture/Hole; Fluid/Blood Leak; Material Puncture/Hole

    THE CUSTOMER REPORTED THAT A NURSE IN THE NICU FOUND A DEFECTIVE OROGASTRIC (OG) TUBE. PER ADDITIONAL INFORMATION PROVIDED BY THE CUSTOMER, THE NURSE PUSHED AIR INTO THE OG ONCE IT WAS INSERTED TO ENSURE IT WAS IN THE PROPER PLACEMENT AND COULD BE HEARD IN THE STOMACH BUT WAS UNABLE TO HEAR THE AIR. THE RN REMOVED THE OG TUBE FROM THE PATIENT AND ATTEMPTED TO PUSH WATER THROUGH THE OG AT THE SINK AREA. THE WATER SQUIRTED OUT OF THE TOP PIECE OF THE PLASTIC JUST BELOW WHERE THE SYRINGE ATTACHES. THE WATER DID NOT TRAVEL THROUGH THE OG, IT ONLY CAME OUT OF THE HOLE AT THE TOP. THE NURSE DISCARDED AND REPLACED THE FEEDING TUBE WITH NO ISSUES. THERE WAS NO PATIENT HARM AND NO CHANGE IN THE MEDICAL TREATMENT/INTERVENTIONS GIVEN.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 12954459 ↗

Other Gastrointestinal Tubes with Enteral Specific Connectors devices

All Gastrointestinal Tubes with Enteral Specific Connectors devices →

Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.