Argyle 8888570507Recalls & 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 10884521050815), received between Jan 10, 2024 and Jan 10, 2024 — 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.

Reports received per month

Last 36 months. The most recent month may be incomplete.

Most reported problems

Device problems

Detachment of Device or Device Component1

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.

MalfunctionJan 10, 2024Detachment of Device or Device Component; Detachment of Device or Device Component
THE CUSTOMER REPORTED THE CHEST TUBE (CT) DISCONNECTED FROM THE TUBING. THE PATIENT'S MOM PRESSED THE CALL BELL WHEN SHE NOTICED, SO IT IS UNKNOWN HOW LONG IT WAS OPEN TO AIR. TPA HAD JUST BEEN INSTILLED APPROXIMATELY 1 HOUR PREVIOUSLY. THERE WAS NO INCREASED WOB OR SIGNS OF RESPIRATORY DISTRESS NOTED AT THE TIME OF DISCOVERY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 18484391 ↗

Device details

UDI-DI	`10884521050815`
Brand	Argyle
Model	8888570507
Company	Cardinal Health, Inc.
Product code	JOL · CATHETER AND TIP, SUCTION
Class	Class 2
FDA submission	None listed
Implant	No
Rx / OTC	Prescription
Single use	Yes
Sterile	Yes
MRI safety	Labeling does not contain MRI Safety Information
Status	Not in Commercial Distribution
Record updated	Jul 30, 2026

Device type (GMDN): Closed-wound drain, non-bioabsorbable

A tube-like, non-bioabsorbable device designed to establish a channel for the removal of fluid or purulent material from a closed-wound or an infected area, typically used with a closed drainage system that applies a low negative pressure through the drain lumen. It is typically made of silicone and comes in various designs/sizes for a variety of surgical applications (e.g., orthopaedic, plastic/reconstructive, neurological, gynaecological, thoracic, cardiovascular, general surgery). It might include disposable devices dedicated to drain insertion/function (e.g., sharp trocar blade, connector), however it does not include any fluid collection bags/containers. This is a single-use device.

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