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SKATER™ All-Purpose and Nephrostomy Drainage Set 756106020Recalls & reported problems

Argon Medical Devices, Inc. · SKATER™ All-Purpose and Nephrostomy Drainage Set Non-Locking 6F x 20cm · Class 1 · Implant

Adverse event reports
1
Deaths reported
0
Injuries reported
1
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00886333225477), received between Oct 4, 2022 and Oct 4, 2022 — classified as 1 injury.

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. How this data works · Data updated Oct 13, 2026.

Most reported problems

Device problems

  • Break1
  • Leak/Splash1

Patient problems

  • Pneumothorax1

Recent adverse event reports

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

  • InjuryOct 4, 2022Break; Leak/Splash

    DRAINAGE CATHETER BROKE AT THE WHITE HUB, DUE TO THE LEAK THE PATIENT HAD A PNEUMOTHORAX. CONNECTING TUBE 404343015, LOT 11410970. REPORT FOR THIS ITEM HAS BEEN PROVIDED AS WELL.

    Patient problems: Pneumothorax

    MAUDE report 15536294 ↗

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