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Argyle 8888160119 (UDI 10884527005093)Recalls & reported problems

Cardinal Health 200, LLC · Polyurethane Umbilical Vessel Catheter Insertion Tray · 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 10884527005093), received between Oct 28, 2019 and Oct 28, 2019 — classified as 1 malfunction.

The most frequently reported specific device problem is “Fluid/Blood Leak” (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

  • Fluid/Blood Leak1

Patient problems

  • No Consequences Or Impact To Patient1

Recent adverse event reports

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

  • MalfunctionOct 28, 2019Fluid/Blood Leak; Fluid/Blood Leak

    AS PER THE CUSTOMER, THE NURSE NOTICED BUBBLING BELOW THE PORTS OF THE UMBILICAL VENOUS CATHETER (UVC). THE CATHETER HAD A HOLE IN IT AND BEING USED ON A PATIENT. THERE WAS NO PATIENT HARM REPORTED.

    Patient problems: No Consequences Or Impact To Patient

    MAUDE report 9244950 ↗

Other CATHETER, UMBILICAL ARTERY devices

All CATHETER, UMBILICAL ARTERY devices →

Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.