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MicroPlex VFC VFC061030-V (UDI 00812636026237)Recalls & reported problems

Microvention, Inc. · V-Trak · Class 2 · Implant

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 00812636026237), received between Jun 22, 2023 and Jun 22, 2023 — classified as 1 malfunction.

The most frequently reported specific device problem is “Premature Separation” (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. How this data works · Data updated Oct 13, 2026.

Most reported problems

Device problems

  • Premature Separation1

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.

  • MalfunctionJun 22, 2023Premature Separation; Premature Separation

    IT WAS REPORTED THAT DURING TREATMENT OF AN ANEURYSM, AN EMBOLIZATION COIL IMPLANT COULD NOT BE ADVANCED OR RETRACTED. THE IMPLANT WAS NOTICED TO HAVE BEEN DETACHED FROM THE PUSHER AND WAS REMOVED ALONG WITH THE MICROCATHETER. THE PROCEDURE WAS SUCCESSFULLY COMPLETED WITH A DIFFERENT COIL. THERE WAS NO INTERVENTION OR INJURY. THE PATIENT WAS REPORTED TO BE "FINE."

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 17183220 ↗

Other DEVICE, NEUROVASCULAR EMBOLIZATION devices

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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.