Victory ™ Victory 18 (300cm, 18g)Recalls & reported problems
Brivant Limited · Class 2
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 08714729826699), received between Nov 24, 2022 and Nov 24, 2022 — classified as 1 malfunction.
The most frequently reported specific device problem is “Difficult to Remove” (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
- Difficult to Remove1
- Flaked1
- Peeled/Delaminated1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionNov 24, 2022Flaked; Peeled/Delaminated; Difficult to Remove; Flaked; Peeled/Delaminated; Difficult to Remove
AS BSC REP WAS NOT PRESENT FOR THE EVENT, THIS IS HOW THE EVENT WAS DESCRIBED: VICTORY 18 WIRE WAS PASSED ACROSS MULTIPLE CHALLENGING LESIONS/CALCIFIC AREAS. NAVICROSS CROSSING CATHETER WAS PASSED OVER THE WIRE, AND WHEN VICTORY 18 WIRE WAS PULLED BACK FOR REMOVAL, THE PHYSICIAN STATED IT FELT AS IF SOMETHING HAD LET LOOSE. UPON PULLING THE VICTORY 18 WIRE OUT OF THE PATIENT, IT WAS NOTICED THAT THE BLUE COATING HAD COME OFF THE WIRE AND WAS NO LONGER PRESENT. PHYSICIAN WAS CONCERNED THAT THE TIP OF THE WIRE HAD COME OFF INSIDE THE PATIENT. IT WAS DECIDED THEN TO REMOVE THE NAVICROSS CROSSING CATH. AND UPON DOING SO, THE BLUE COATING WAS LITERALLY HANGING FROM THE TIP OF THE NAVICROSS. BSC REP'S UNDERSTANDING IS THAT THE NAVICROSS WAS IN FACT AN .018, SO SIZING HERE SHOULD NOT HAVE BEEN AN ISSUE. SOUNDS AS IF COATING ON THE VICTORY WIRE CAME OFF POTENTIALLY AFTER CROSSING MULTIPLE CHALLENGING LESIONS OR DIFFICULT CALCIFIED AREAS. BSC REP WAS NOT PRESENT DURING THIS PROCEDURE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 15860699 ↗
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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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