Valiant Navion™ VNMC3131C223TU (UDI 00763000260781)Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00763000260781), received between Jun 30, 2023 and Jun 30, 2023 — classified as 1 malfunction.

The most frequently reported specific device problem is “Detachment of Device or Device Component” (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

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

• MalfunctionJun 30, 2023Detachment of Device or Device Component; Detachment of Device or Device Component

  A VALIANT NAVION STENT GRAFT WAS IMPLANTED IN AN UNKNOWN ENDOVASCULAR PROCEDURE.  IT WAS REPORTED THAT CT IMAGING WAS PERFORMED ON (B)(6) 2022. CORELAB HAVE REVIEWED THIS IMAGING AND IDENTIFIED STENT RING ENLARGEMENT OF + 1.2MM ON RING 7 OF THE VALIANT NAVION.  NO ENDOLEAK, FRACTURE OR STENT RING MIGRATION WERE NOTED. THE MAXIMUM AORTIC DIAMETER MEASURED 45.2MM.  NO AORTIC ENLARGEMENT WAS NOTED.  NO CAUSE WAS REPORTED.  NO ADDITIONAL CLINICAL SEQUALAE WERE PROVIDED AND THE PATIENT WILL BE MONITORED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 17237752 ↗