Victory ™ Victory 14 (300cm, 18g)Recalls & reported problems
Brivant Limited · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 08714729826613), received between Jun 27, 2023 and Jan 9, 2024 — classified as 2 malfunctions.
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.
Reports received per month
Most reported problems
Device problems
- Difficult to Remove1
- Fracture1
Patient problems
- No Clinical Signs, Symptoms or Conditions2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionJan 9, 2024Difficult to Remove; Difficult to Remove
THE DOCTORS WERE TRYING TO ACCESS THE ANTERIOR TIBIAL ARTERY FROM THE POPLITEAL ARTERY AND WEREN´T ABLE TO. THEY TOOK OUT THE VICTORY GUIDEWIRE OUT OF THE BALLOON TO INSERT ANOTHER WIRE WHEN THEY NOTICED THAT THE TIP OF THE VICTORY GUIDEWIRE WAS STUCK IN THE HUB. WHAT TROUBLESHOOTING STEPS TOOK PLACE? WHAT TROUBLESHOOTING STEPS, IF ANY, RESOLVED THE ISSUE?: THEY TRIED TO DISLODGE THE STUCK TIP BY INJECTING SALINE SOLUTION INTO THE BALLOON AND ALSO PUSH IT WITH ANOTHER GUIDEWIRE. WHAT IS THE NEXT COURSE OF ACTION?: NONE PATIENT PRESENT AT TIME OF EVENT?: YES PATIENT COMPLICATIONS: NO PATIENT COMPLICATIONS DEVICE ACQUIRED FROM A DISTRIBUTOR?: NO.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 18473711 ↗MalfunctionJun 27, 2023Fracture; Fracture
IT IS BROKEN CATHETER CANNOT BE PUSHED. WHAT TROUBLESHOOTING STEPS TOOK PLACE? WHAT TROUBLESHOOTING STEPS, IF ANY, RESOLVED THE ISSUE?: IT IS BROKEN CATHETER CANNOT BE PUSHED. WHAT IS THE NEXT COURSE OF ACTION?: THEY NEED A NEW VICTORY 14 PATIENT PRESENT AT TIME OF EVENT?: YES PATIENT COMPLICATIONS: NO PATIENT COMPLICATIONS REASON FOR UNSUCCESSFUL PROCEDURE: IT IS BROKEN CATHETER CANNOT BE PUSHED. BASED ON THE OUTCOME NOTED ABOVE, WAS THE PATIENT SEDATED WHEN THE PROCEDURE WAS CANCELED?: YES - LOCAL ANESTHESIA DEVICE ACQUIRED FROM A DISTRIBUTOR?: NO.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17207899 ↗
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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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