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Argyle 8888570572Recalls & reported problems

Cardinal Health, Inc. · Thoracic Catheter,Straight · Class 2

Adverse event reports
1
Deaths reported
0
Injuries reported
1
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10884521050877), received between Mar 19, 2021 and Mar 19, 2021 — classified as 1 injury.

The most frequently reported specific device problem is “Break” (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

  • Break1

Patient problems

  • Insufficient Information1

Recent adverse event reports

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

  • InjuryMar 19, 2021Break; Break

    THE CUSTOMER REPORTED THE DRAIN TORE WHEN IT PASSED THE BREASTBONE IN PREPARATION FOR HEART SURGERY. A PIECE OF THE DRAIN CAME OFF AS THEY USED A PAIR OF PLIERS TO PUSH IT THROUGH THE BREASTBONE. THE DOCTOR STATED THAT HE WOULD RATHER HAVE A RIGID TUBE THAN THE FLEXIBLE ONE.

    Patient problems: Insufficient Information

    MAUDE report 11526169 ↗

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.