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Argyle 8888570523Recalls & reported problems

Cardinal Health, Inc. · Thoracic Catheter,Straight · 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 10884521050839), received between Apr 3, 2023 and Apr 3, 2023 — classified as 1 malfunction.

The most frequently reported specific device problem is “Failure to Disconnect” (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

  • Failure to Disconnect1

Patient problems

  • Insufficient Information1
  • 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.

  • MalfunctionApr 3, 2023Failure to Disconnect; Failure to Disconnect

    THE CUSTOMER REPORTED THAT WHEN PERFORMING PLEURAL DRAINAGE FOR A PNEUMOTHORAX IN A PATIENT, IT WAS IMPOSSIBLE TO REMOVE THE TROCAR USED TO PLACE THE DRAIN. INDEED, THE DIAMETER OF THE DRAIN IS LARGER AT THE DISTAL END, WHICH MADE IT IMPOSSIBLE TO REMOVE THE TROCAR. CONSEQUENCES WERE LISTED AS ENDANGERMENT OF THE PATIENT, UNSTABLE STATE AND HYPOXEMIC PATIENT.

    Patient problems: Insufficient Information; No Clinical Signs, Symptoms or Conditions

    MAUDE report 16668203 ↗

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.