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Argyle 460604Recalls & reported problems

Cardinal Health 200, LLC · Feeding Tube • Radiopaque · 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 10884521067325), received between Jun 13, 2019 and Aug 27, 2020 — classified as 2 malfunctions.

The most frequently reported specific device problem is “Break” (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

  • Break1
  • Material Perforation1

Patient problems

  • No Known Impact Or Consequence To Patient1
  • No Patient Involvement1

Recent adverse event reports

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

  • MalfunctionAug 27, 2020Material Perforation; Material Perforation

    CUSTOMER REPORTS: THE TUBE HAS A HOLE IN THE TOP BY THE PURPLE PORT WHERE THE SYRINGE ATTACHES.

    Patient problems: No Known Impact Or Consequence To Patient

    MAUDE report 10459849 ↗
  • MalfunctionJun 13, 2019Break; Break

    THE CUSTOMER STATES THAT THE FEEDING TUBE WAS FOUND BROKEN IN HALF INSIDE THE PACKAGING.

    Patient problems: No Patient Involvement

    MAUDE report 8696266 ↗

Other TUBES, GASTROINTESTINAL (AND ACCESSORIES) devices

All TUBES, GASTROINTESTINAL (AND ACCESSORIES) devices →

Sources and updates

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