Renegade™ STC 18 M001181340Recalls & reported problems
Boston Scientific Corporation · Microcatheter · Class 2
All models of Renegade STC 18 (7)
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 08714729444473), received between Sep 5, 2019 and Sep 5, 2019 — 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 Patient Involvement1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 5, 2019Break; Break
IT WAS REPORTED THAT THE DEVICE CAME OUT IN TWO PIECES. A RENEGADE STC-18 WAS SELECTED FOR USE. UPON PREPARATION, THE DEVICE CAME OUT IN TWO PIECES WHEN TAKEN OUT OF THE HOOP AND NEVER ENTERED THE PATIENT'S BODY. THE DEVICE WAS SEVERED ABOUT 10 INCHES BELOW THE WIRE AND FLUSHED PORT. THE PROCEDURE WAS COMPLETED WITH ANOTHER OF THE SAME DEVICE. NO COMPLICATIONS REPORTED AND PATIENT IS FINE.
Patient problems: No Patient Involvement
MAUDE report 8966480 ↗
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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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