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ArgoTrans Model 2 041586505ARecalls & reported problems

Argon Medical Devices, Inc. · ArgoTrans Model 2, 3ml Micro, 9" Ext, 6" Line Stopcock · 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 00886333201754), received between Aug 29, 2019 and Aug 29, 2019 — classified as 1 malfunction.

The most frequently reported specific device problem is “Mechanical Problem” (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

  • Mechanical Problem1

Patient problems

  • Atrial Flutter1
  • Chronic Obstructive Pulmonary Disease (COPD)1
  • Pneumothorax1

Recent adverse event reports

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

  • MalfunctionAug 29, 2019Mechanical Problem; Mechanical Problem

    LEFT RADIAL ARTERIAL LINE IN PLACE DRAWING BLOOD FROM THE PROXIMAL PORT. LEAKING BEGAN FROM BACKSIDE OF THE THREE WAY STOP COCK WHEN BLOOD WAS PULLED INTO THE SYRINGE. BLOOD FLOWED SLOWLY THEN VERY QUICKLY FROM THE BACKSIDE. IT APPEARED A SMALL WHITE PLUG WAS MISSING OR A MFR ERROR WITH DEVICE.

    Patient problems: Atrial Flutter; Chronic Obstructive Pulmonary Disease (COPD); Pneumothorax

    MAUDE report 8957205 ↗

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