Skip to content

SKATER™ Drainage Catheter 755114025ERecalls & reported problems

Argon Medical Devices, Inc. · SKATER™ Drainage Catheter - locking pigtail 14F x 25cm · Class 1

All models of SKATER Drainage Catheter (5)

Data updated Oct 18, 2026 from official FDA records · Editorial policy

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 00886333001194), received between Dec 13, 2021 and Dec 13, 2021 — classified as 1 malfunction.

The most frequently reported specific device problem is “Fluid/Blood Leak” (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 18, 2026.

Most reported problems

Device problems

  • Fluid/Blood Leak1

Patient problems

  • Insufficient Information1

Recent adverse event reports

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

  • MalfunctionDec 13, 2021Fluid/Blood Leak

    AFTER PLACING THE PIGTAIL IN THE VIVO THE OPERATORS FOUND THE STRING PORT OF THE HUB WAS KEEPING LEAKED.

    Patient problems: Insufficient Information

    MAUDE report 12987421 ↗

Other Catheter, Continuous Irrigation devices

All Catheter, Continuous Irrigation devices →

Sources and updates

How reports and recalls are matched · Editorial policy · Report an error on this page