SKATER™ All Purpose and Nephrostomy Drainage Set 756107025Recalls & reported problems
Argon Medical Devices, Inc. · SKATER™ All Purpose and Nephrostomy Drainage Set Non-Locking 7F x 25cm · Class 1 · Implant
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 00886333225507), received between Mar 7, 2023 and Mar 7, 2023 — classified as 1 malfunction.
The most frequently reported specific device problem is “Crack” (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
- Crack1
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 7, 2023Crack; Crack
ON (B)(6) 2023, THE PATIENT UNDERWENT KIDNEY PUNCTURE AND DRAINAGE UNDER B-ULTRASOUND GUIDANCE DUE TO HYDRONEPHROSIS. AFTER THE DOCTOR PLACED THE TUBE SUCCESSFULLY THAT DAY, HE FOUND THAT THERE WAS A CRACK AT THE INTERFACE OF THE DRAINAGE TUBE, WHICH WAS COVERED BY OTHER PARTS BEFORE OPERATION AND COULD NOT BE TESTED. THE DOCTOR IMMEDIATELY STRENGTHENED THE FIXATION WITH ADHESIVE TAPE FOR REMEDY, BUT THERE WAS A RISK OF INCREASING INFECTION, AND IMMEDIATELY REPORTED ADVERSE EVENTS.
Patient problems: Insufficient Information
MAUDE report 16496153 ↗
Other Catheter, Nephrostomy, General & Plastic Surgery devices
- NA M0067001210Boston Scientific Corporation · CATHETER, NEPHROSTOMY, GENERAL & PLASTIC SURGERY2 deaths48 reports
- NA M0064201110Boston Scientific Corporation · CATHETER, NEPHROSTOMY, GENERAL & PLASTIC SURGERY6 reports
- Flexima™ M001271800Boston Scientific Corporation · CATHETER, NEPHROSTOMY, GENERAL & PLASTIC SURGERY6 reports
- Skater™ All-Purpose and Nephrostomy Set 756608025Argon Medical Devices, Inc. · Catheter, Nephrostomy, General & Plastic Surgery5 reports
- Flexima™ M001271790Boston Scientific Corporation · CATHETER, NEPHROSTOMY, GENERAL & PLASTIC SURGERY4 reports
- Re-Entry Malecot Nephrostomy Catheter Set M0064101060Boston Scientific Corporation · CATHETER, NEPHROSTOMY, GENERAL & PLASTIC SURGERY4 reports
- SKATER™ All Purpose and Nephrostomy Drainage Set 756608035Argon Medical Devices, Inc. · Catheter, Nephrostomy, General & Plastic Surgery4 reports
- Flexima™ M001271860Boston Scientific Corporation · CATHETER, NEPHROSTOMY, GENERAL & PLASTIC SURGERY2 reports
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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