VIA Microcatheter VIA-27-154-01-MVI2Recalls & reported problems

Summary

The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 00842429106426), received between Jun 18, 2021 and May 30, 2025 — classified as 2 injuries, 1 malfunction.

The most frequently reported specific device problem is “Peeled/Delaminated” (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 3 most recent of 3 reports, in the reporter's own words as published by the FDA.

• MalfunctionMay 30, 2025Peeled/Delaminated; Peeled/Delaminated

  ADDITIONAL INFORMATION WAS RECEIVED THAT STATED IT HAPPENED WHILE INSERTING THE VIA INTO THE HUB. AFTER THAT, THEY TOOK ANOTHER VIA AND USED IT WITH THE WEB TO COMPLETE THE CASE. THERE WERE NO PICTURES TAKEN OF THE SEGMENT THAT WAS IN THE CATHETER HUB.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22118025 ↗
• InjuryOct 6, 2022Unintended Movement; Unintended Movement

  IT WAS REPORTED THAT WHEN ADVANCING A WEB DEVICE THROUGH THE VIA 27 DURING THE TREATMENT OF AN ANTERIOR COMMUNICATING ARTERY (ACOM) ANEURYSM, THE VIA CATHETER SHIFTED FORWARD AND PERFORATED THE DOME OF THE ANEURYSM, RESULTING IN BLEEDING INTO THE BRAIN. THE VIA AND WEB DEVICE WERE REMOVED, AND THE RUPTURED ANEURYSM WAS TREATED WITH COILS. THE PATIENT WAS BEING MONITORED IN THE ICU AND REPORTED TO BE NEUROLOGICALLY INTACT AND HAD A HEADACHE. THERE WERE NO FOCAL DEFICITS OR HYDROCEPHALUS, AND THE BLOOD IS CLEARING UP ON CT HEAD.

  Patient problems: Headache; Hemorrhage/Blood Loss/Bleeding; Ruptured Aneurysm

  MAUDE report 15556223 ↗
• InjuryJun 18, 2021Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT DURING TREATMENT OF AN ANEURYSM, A VIA MICROCATHETER AND WEB DEVICE WERE ADVANCED INTO POSITION WHEN AN ANGIOGRAPHIC RUN REVEALED EXTRAVASATION. IT WAS NOT KNOWN IF THE WEB OR THE VIA CAUSED THE EXTRAVASATION. HEPARIN WAS REVERSED AND THE NEXT ANGIOGRAPHIC RUN REVEALED NO FURTHER EXTRAVASATION. THE WEB WAS IMPEDING FLOW IN THE PARENT VESSEL. A COMPETITOR'S STENT WAS PLACED IN ORDER TO KEEP THE WEB DEVICE IN THE ANEURYSM. FLOW THROUGH THE STENT SHUT DOWN AND INTEGRILIN WAS ADMINISTERED, WHICH RESTORED FLOW. POST PROCEDURE, THE PATIENT WAS AWAKE, FOLLOWING COMMANDS AND MOVING THEIR RIGHT AND LEFT LEGS. THERE WAS NO REPORTED SEQUELAE.

  Patient problems: Extravasation

  MAUDE report 12029483 ↗