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SKATER™ Drainage Catheter 755106025ERecalls & reported problems

Argon Medical Devices, Inc. · SKATER™ Drainage Catheter - locking pigtail 6F 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 00886333000111), received between Mar 28, 2023 and Mar 28, 2023 — classified as 1 malfunction.

The most frequently reported specific device problem is “Difficult to Remove” (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

  • Difficult to Remove1
  • Physical Resistance/Sticking1

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.

  • MalfunctionMar 28, 2023Difficult to Remove; Physical Resistance/Sticking; Difficult to Remove; Physical Resistance/Sticking

    THE NEEDLE CORE COULD NOT BE PULLED OUT AFTER THE RENAL CYST DRAINAGE TUBE WAS PLACED, RESULTING IN A PILE OF TUBES AT THE END OF THE DRAINAGE TUBE, AND THE PATIENT COULD NOT BE TREATED AFTER REMOVAL.

    Patient problems: Insufficient Information

    MAUDE report 16628762 ↗

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Sources and updates

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