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Skater™ All-Purpose and Nephrostomy Drainage Set 756612025Recalls & reported problems

Argon Medical Devices, Inc. · Skater™ All-Purpose and Nephrostomy Drainage Set – Locking 12Fr x 25cm · Class 1

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 00886333217847), received between Sep 13, 2022 and Sep 13, 2022 — classified as 1 malfunction.

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 18, 2026.

Most reported problems

Device problems

  • Break1

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.

  • MalfunctionSep 13, 2022Break

    WHILE PLACING THE SKATER DRAINAGE CATHETER, THE LOCKING MECHANISM BROKE, CATHTER WAS REMOVED AND A NEW CATHETER HAD TO BE PLACED FOR THE PATIENT.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 15410715 ↗

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Sources and updates

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