Argyle 460208ERecalls & reported problems
Cardinal Health, Inc. · 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 10884521547186), received between Oct 10, 2024 and Oct 10, 2024 — classified as 1 malfunction.
The most frequently reported specific device problem is “Material Separation” (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.
Reports received per month
Most reported problems
Device problems
- Material Separation1
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.
MalfunctionOct 10, 2024Material Separation; Material Separation
THE CUSTOMER REPORTED A 10 FR ARGYLE FEEDING TUBE WAS FOUND TO BE SEVERED IN TWO PIECES INSIDE THE PACKAGE (UNUSED). NO OTHER DEFECTIVE TUBES HAVE BEEN FOUND. A SAFETY REPORT WAS NOT ENTERED. THE ISSUE WAS FOUND OVER THE WEEKEND AND THE TUBE WAS KEPT. IT¿S ODD IN THAT THE ENDS DO NOT APPEAR TO ALIGN WHERE IT APPEARS SEVERED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20420996 ↗
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.