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Kangaroo 461503Recalls & reported problems

Cardinal Health 200, LLC · Radiopaque Line, Safe Enteral Connections · Class 2

Adverse event reports
6
Deaths reported
0
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 6 adverse event reports that list this exact device (DI 10884521067974), received between Apr 13, 2018 and Jul 14, 2023 — classified as 6 malfunctions.

The most frequently reported specific device problem is “Detachment of Device or Device Component” (3 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

  • Detachment of Device or Device Component3
  • Break1
  • Material Split, Cut or Torn1
  • Occlusion Within Device1

Patient problems

  • No Clinical Signs, Symptoms or Conditions2
  • No Known Impact Or Consequence To Patient2
  • No Consequences Or Impact To Patient1
  • No Patient Involvement1

Recent adverse event reports

The 6 most recent of 6 reports, in the reporter's own words as published by the FDA.

  • MalfunctionJul 14, 2023Detachment of Device or Device Component; Detachment of Device or Device Component

    CUSTOMER REPORTS: THE PURPLE END TIP POPPED OFF FROM THE INSERTED 5FRENCH 36 FEEDING TUBE BEING USED ON A BABY FOR FEEDS. THE TUBE WAS REMOVED IMMEDIATELY WITH NO KNOWN CONCERNS TO PATIENT. LOT NUMBERS THAT WERE AVAILABLE AT THE UNIT ARE LOT #S 2231310564 OR #2215831164.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 17326690 ↗
  • MalfunctionJul 7, 2023Material Split, Cut or Torn; Material Split, Cut or Torn

    CUSTOMER REPORTS: THE TUBE WAS GOING TO BE REPLACED WITH LOT #2231310564 BUT THE REPLACEMENT TUBE WAS SPLIT IN TWO AND NOT USED.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 17283437 ↗
  • MalfunctionJul 24, 2020Detachment of Device or Device Component; Detachment of Device or Device Component

    CUSTOMER REPORTS: THE END CAP OF THE FEEDING TUBE BROKE OFF DURING USE.

    Patient problems: No Known Impact Or Consequence To Patient

    MAUDE report 10320075 ↗
  • MalfunctionJul 24, 2020Detachment of Device or Device Component; Detachment of Device or Device Component

    THE CUSTOMER REPORTED THAT THE PURPLE CONNECTOR HAD SEPARATED FROM THE TUBING.

    Patient problems: No Known Impact Or Consequence To Patient

    MAUDE report 10319950 ↗
  • MalfunctionMar 2, 2020Break; Break

    THE CUSTOMER REPORTED THAT THE NASOGASTRIC TUBE WAS BROKEN AT THE HUB WHERE THE FEEDING BAG TUBING CONNECTS. THERE WAS NO PATIENT INJURY.

    Patient problems: No Consequences Or Impact To Patient

    MAUDE report 9777000 ↗
  • MalfunctionApr 13, 2018Occlusion Within Device; Occlusion Within Device

    THE CUSTOMER REPORTED THE FEEDING TUBE IS FUSED TOGETHER AROUND THE MIDDLE OF THE TUBING. THERE WAS NO PATIENT INVOLVED.

    Patient problems: No Patient Involvement

    MAUDE report 7429323 ↗

Other TUBES, GASTROINTESTINAL (AND ACCESSORIES) devices

All TUBES, GASTROINTESTINAL (AND ACCESSORIES) devices →

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