VIA Microcatheter VIA-17-154-90-ALRecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00842429118757), received between Aug 27, 2025 and Aug 27, 2025 — classified as 1 death.

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. How this data works · Data updated Oct 13, 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.

• DeathAug 27, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED TO MICROVENTION THAT THE PATIENT WAS INTUBATED AND UNDER GENERAL ANESTHESIA, NOT UNDER CONSCIOUS SEDATION, FOR AN OFF-LABEL USE OF THE WEB IN A PARAOPHTHALMIC ANEURYSM. THE PATIENT WAS REPORTED TO HAVE COUGHED OVER THEIR ET TUBE. THIS REPORTEDLY CAUSED THE SYSTEM OF CATHETERS USED FOR TREATMENT, INCLUDING THE SOFIA, VIA, AND ¿OTHER DEVICES¿, TO MOVE UNEXPECTEDLY. THESE DEVICES WERE IN THE PATIENT WHEN IT WAS THEN NOTICED THAT THE VESSEL WAS PERFORATED. A WEB DEVICE WAS THEN INSERTED AFTER THE PERFORATION AND REPORTEDLY DID NOT INITIALLY DETACH. THE 90 DEGREE VIA WAS BROUGHT UP TO BRACE AGAINST THE WEB TO DETACH AND THE WEB CAME TO REST IN THE PARENT VESSEL. INTERVENTION WITH SNARE AND TWO OTHER DEVICES WERE USED IN AN ATTEMPT TO RETRIEVE THE WEB, WHICH PROVED UNSUCCESSFUL. THE CASE WAS TERMINATED DUE TO THE VESSEL WALL BLEEDING, AND THE WEB REMAINED IN THE PARENT VESSEL. THE PATIENT PASSED AWAY THE NEXT DAY. THIS WEB DEVICE USED IN THIS CASE WAS SUBMITTED UNDER MDR 2032493-2025-90428.

  Patient problems: Ruptured Aneurysm

  MAUDE report 22908296 ↗