TrailBlazer™ Angled ASC-014-150Recalls & reported problems
Covidien LP · PS ASC-014-150 TRAILBLAZER ANGLED V03 · Class 2
Data updated Oct 16, 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 00763000104665), received between Feb 21, 2020 and Feb 21, 2020 — classified as 1 malfunction.
The most frequently reported specific device problem is “Device Damaged by Another Device” (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 16, 2026.
Most reported problems
Device problems
- Device Damaged by Another Device1
Patient problems
- No Known Impact Or Consequence To Patient1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionFeb 21, 2020Device Damaged by Another Device; Device Damaged by Another Device
PHYSICIAN INTENDED TO USE AN ANGLED TRAILBLAZER DURING PATIENT TREATMENT. IFU WAS FOLLOWED. A BROKEN CATHETER IS REPORTED. IT IS REP ORTED THE WIRE RUPTURED THROUGH THE WALL OF THE CATHETER. NO CATHETER SEGMENTS ARE REPORTED TO HAVE BEEN STUCK ON THE GUIDEWIRE. ANOTHER CATHETER WAS USED TO COMPLETE THE PROCEDURE. PATIENT STATUS UNKNOWN. NO INJURY REPORTED.
Patient problems: No Known Impact Or Consequence To Patient
MAUDE report 9738552 ↗
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- Guidezilla™ H7493924215050Boston Scientific Corporation · CATHETER, PERCUTANEOUS294 reports
- WATCHMAN™ TruSeal™ Access System M635TU70020Boston Scientific Corporation · Catheter, percutaneous1 recall11 deaths217 reports
- Lantern Delivery Catheter PXSLIMLAN135T45Penumbra, Inc. · CATHETER, PERCUTANEOUS220 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 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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