Argyle 461206ERecalls & 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 10884521547247), received between May 26, 2026 and May 26, 2026 — 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.
MalfunctionMay 26, 2026Material Separation
THE CUSTOMER REPORTED THEY NEEDED A FEEDING TUBE AND WHEN GRABBING THIS FEEDING TUBE THE WRITER NOTICED THAT THE TIP LOOKED FLAT/PINCHED. AFTER INSPECTING IT FURTHER, IT IS NOT THE LENGTH THAT IT SHOULD BE, THE LAST FEW CENTIMETERS ARE NOT THERE. IT IS CUT OFF AT THE 8 CM MARK AND FLATTENED. THE WRITER OPENED THE PACKAGE, ATTACHED AN ENFIT SYRINGE AND TRIED TO PASS AIR THROUGH THE TUBING, NO AIR OR FLUID CAN PASS THROUGH THE TUBE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25281937 ↗
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.