Skip to content

Argyle 31400Recalls & reported problems

Cardinal Health, Inc. · Suction Catheter with Chimney Valve,Straight Packed · 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 10884527002153), received between Mar 19, 2020 and Mar 19, 2020 — 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 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.

  • MalfunctionMar 19, 2020Detachment of Device or Device Component; Detachment of Device or Device Component

    THE CUSTOMER REPORTED THAT THE DEVICE WAS OPENED TO SUCTION THE PATIENT'S TRACH, AND IT WAS FOUND THAT THE TIP OF THE CATHETER WAS DETACHED IN THE PACKAGE. THERE WAS NO PATIENT INVOLVEMENT.

    Patient problems: No Consequences Or Impact To Patient

    MAUDE report 9853476 ↗

Other CATHETER AND TIP, SUCTION devices

All CATHETER AND TIP, SUCTION devices →

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