Skater™ Centesis Catheter 700305010Recalls & reported problems
Argon Medical Devices, Inc. · Skater™ Centesis Catheter 5Fr x 10cm · Class 1
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00886333005802), received between May 10, 2023 and May 19, 2023 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Air/Gas in Device” (2 reports).
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
- Air/Gas in Device2
Patient problems
- Insufficient Information2
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionMay 19, 2023Air/Gas in Device; Air/Gas in Device
SEEMS TO BE DRAWING AIR FROM SOMEWHERE, THE ACCOUNT BELIEVES IT IS FROM A VERY SPECIFIC SPOT BELOW THE HUB. VIDEOS AND PICTURE ARE ATTACHED.
Patient problems: Insufficient Information
MAUDE report 16963583 ↗MalfunctionMay 10, 2023Air/Gas in Device; Air/Gas in Device
SEEMS TO BE DRAWING AIR FROM SOMEWHERE, THE ACCOUNT BELIEVES IT IS FROM A VERY SPECIFIC SPOT BELOW THE HUB. VIDEOS AND PICTURE ARE ATTACHED.
Patient problems: Insufficient Information; No Clinical Signs, Symptoms or Conditions
MAUDE report 16902469 ↗
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- Skater™ Centesis Catheter 700304015Argon 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.
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