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MicroPlex Complex 100718CC-VRecalls & 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 00810170010460), received between Aug 2, 2023 and Aug 2, 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.

  • MalfunctionAug 2, 2023Premature Separation; Premature Separation

    IT WAS REPORTED THAT DURING A COIL EMBOLIZATION PROCEDURE, THE COIL PREMATURELY DETACHED. THE COIL AND MICROCATHETER WERE BOTH REMOVED FROM THE PATIENT. THERE WAS NO PATIENT INJURY OR INTERVENTION.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 17446500 ↗

Other DEVICE, NEUROVASCULAR EMBOLIZATION devices

All DEVICE, NEUROVASCULAR EMBOLIZATION devices →

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