Argyle 460711Recalls & 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
- 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 10884521067349), received between Sep 25, 2024 and Sep 25, 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.
MalfunctionSep 25, 2024Material Separation; Material Separation
THE CUSTOMER REPORTED THEY HAVE A PRODUCT COMPLAINT WITH 7 EACHES OF 460711 6.5FR ARGYLE FEEDING TUBE LOT NUMBER 2215833464. ONE OF THE PRODUCTS WAS SEALED WITH PART OF THE PRODUCT CUT OFF OUTSIDE THE PACKAGE. WITH THE OTHER SIX, THE TUBE WAS SPLIT IN TWO PIECES INSIDE THE PACKAGE. PHOTOS ATTACHED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 20305996 ↗
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Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 13, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 13, 2026
- Page last rebuilt: Oct 13, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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