Argyle 8888572545Recalls & reported problems
Cardinal Health, Inc. · Silicone Thoracic Catheter Straight · Class 1
All models of Argyle (64)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- 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 10884521025455), received between May 6, 2017 and May 6, 2017 — 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. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.
Most reported problems
Device problems
- Break1
Patient problems
- Device Embedded In Tissue or Plaque1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryMay 6, 2017Break; Break
THE CUSTOMER REPORTS THE DOCTOR HAD PLACED THE CHEST TUBE DURING OPEN HEART AND WAS BEING REMOVED ON (B)(6) 2017 WHEN IT BROKE OFF INTO THE PATIENT. THE CUSTOMER FURTHER REPORTS THEY HAD TO DO SURGERY TO REMOVE THE BROKEN CATHETER.
Patient problems: Device Embedded In Tissue or Plaque
MAUDE report 6550785 ↗
Other CATHETER, VENTRICULAR, GENERAL & PLASTIC SURGERY devices
- Thoracic Drain TC-xxxxxLivanova USA, Inc. · CATHETER, VENTRICULAR, GENERAL & PLASTIC SURGERY5 reports
- Argyle 8888572552Cardinal Health, Inc. · CATHETER, VENTRICULAR, GENERAL & PLASTIC SURGERY2 reports
- Argyle 8888573048Cardinal Health, Inc. · CATHETER, VENTRICULAR, GENERAL & PLASTIC SURGERY1 report
- Axiom® Atraum™ With ClotStop® 111120ATAxiom Medical, Incorporated · Catheter, Ventricular, General & Plastic Surgery1 report
- Argyle 8888572560Cardinal Health, Inc. · CATHETER, VENTRICULAR, GENERAL & PLASTIC SURGERY1 report
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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