Renegade™ STC 18 M001181250Recalls & 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 08714729444381), received between Aug 15, 2019 and Aug 15, 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.
MalfunctionAug 15, 2019Break; Break
IT WAS REPORTED THAT CATHETER TIP WAS BROKEN. A 105/20/STRAIGHT/1RO RENEGADE STC 18 WAS SELECTED FOR USE. DURING PREPARATION, IT WAS NOTED THAT THE TIP WAS BROKEN AND THE DEVICE WAS CRACKED WHEN UNPACKING. THE DEVICE WAS NOT USED WITHIN THE PATIENT. NO PATIENT COMPLICATIONS REPORTED.
Patient problems: No Patient Involvement
MAUDE report 8896517 ↗
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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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