Skip to content

Argyle 461206Recalls & reported problems

Cardinal Health 200, LLC · Premature Infant Feeding Tube • Radiopaque · Class 2

Adverse event reports
1
Deaths reported
0
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10884521067387), received between Nov 8, 2022 and Nov 8, 2022 — classified as 1 malfunction.

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

  • Detachment of Device or Device Component1

Patient problems

  • No Clinical Signs, Symptoms or Conditions1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • MalfunctionNov 8, 2022Detachment of Device or Device Component; Detachment of Device or Device Component

    CUSTOMER REPORTS: THE GREEN CAP DISCONNECTED FROM THE FEEDING TUBE, LEAVING ONLY THE SMALL TUBING IN THE BABY HANGING OUT. THIS POSES A RISK OF INFECTION AND ASPIRATION. PER ADDITIONAL INFORMATION RECEIVED ON 11/08/22, THERE WAS NO HARM. THE DEVICE WAS REPLACED AND THE PATIENT WAS DISCHARGED HOME.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 15754230 ↗

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.