Skater™ Centesis Catheter 700304015Recalls & reported problems
Argon Medical Devices, Inc. · Skater™ Centesis Catheter 4Fr x 15cm · 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 00886333005789), received between Aug 18, 2022 and Aug 18, 2022 — classified as 1 malfunction.
The most frequently reported specific device problem is “Separation Failure” (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
- Separation Failure1
- Therapeutic or Diagnostic Output Failure1
Patient problems
- Obstruction/Occlusion1
- Pain1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionAug 18, 2022Separation Failure; Therapeutic or Diagnostic Output Failure
ON (B)(6) 2022, THE PATIENT WAS ADMITTED TO THE HOSPITAL FOR 3 DAYS DUE TO THE STONE IN THE MIDDLE AND LOWER SEGMENT OF THE LEFT URETER WITH LEFT HYDRONEPHROSIS. THE DOCTOR PERFORMED THE KIDNEY DRAINAGE TUBE PLACEMENT UNDER THE GUIDANCE OF B-ULTRASOUND. THE DOCTOR USED THE DRAINAGE TUBE AND ACCESSORIES FOR PUNCTURE AND DRAINAGE. DURING THE OPERATION, IT WAS FOUND THAT THE DRAINAGE TUBE AND THE NEEDLE CORE COULD NOT BE SEPARATED, AND NO EFFUSION WAS DRAINED AFTER THE TUBE PLACEMENT. IT WILL AFFECT THE OPERATION EFFECT AND INCREASE THE PATIENT'S PAIN.
Patient problems: Obstruction/Occlusion; Pain
MAUDE report 15249758 ↗
Other Catheter, Continuous Irrigation devices
- SKATER™ Drainage Catheter 755108035EArgon Medical Devices, Inc. · Catheter, Continuous Irrigation17 reports
- SKATER™ Drainage Catheter 755108025EArgon Medical Devices, Inc. · Catheter, Continuous Irrigation3 reports
- Skater™ Centesis Catheter 700305010Argon Medical Devices, Inc. · Catheter, Continuous Irrigation2 reports
- SKATER™ Single Step Drainage Set 756006025EArgon Medical Devices, Inc. · Catheter, Continuous Irrigation1 report
- SKATER™ Drainage Catheter 755106025EArgon Medical Devices, Inc. · Catheter, Continuous Irrigation1 report
- SKATER™ Drainage Catheter 751108025EArgon Medical Devices, Inc. · Catheter, Continuous Irrigation1 report
- SKATER™ Drainage Catheter 755114025EArgon Medical Devices, Inc. · Catheter, Continuous Irrigation1 report
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
How reports and recalls are matched · Editorial policy · Report an error on this page