Skip to content

Argyle 8888571034Recalls & reported problems

Cardinal Health, Inc. · Thoracic Catheter,Right Angle · Class 2 · Implant

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 10884521050907), received between Feb 9, 2023 and Feb 9, 2023 — classified as 1 malfunction.

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

  • 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.

  • MalfunctionFeb 9, 2023Break; Break

    THE CUSTOMER REPORTED THAT THE PATIENT HAD MEDIASTINAL DRAINS AFTER HEART SURGERY. ACTIVE BLEEDING WAS PRESENT IN THE RETROCARDIAC DRAIN AND EXTENSIVE MILKING WITH FORCEPS WAS REQUIRED. PER CUSTOMER, THE RETRO CARDIAC DRAIN WAS CRACKED AT THE JOINT AND WAS READY TO RUPTURE. THERE WAS NO HARM REPORTED.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 16336714 ↗

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.