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MicroPlex Cosmos 180723CS-VRecalls & reported problems

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

Adverse event reports
1
Deaths reported
0
Injuries reported
1
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00810170014055), received between Feb 27, 2020 and Feb 27, 2020 — classified as 1 injury.

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. How this data works · Data updated Oct 13, 2026.

Most reported problems

Device problems

  • Detachment of Device or Device Component1

Patient problems

  • No Consequences Or Impact To Patient1

Recent adverse event reports

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

  • InjuryFeb 27, 2020Detachment of Device or Device Component; Detachment of Device or Device Component

    IT WAS REPORTED THAT TREATMENT WAS PERFORMED ON A RUPTURED INTERNAL CAROTID ARTERY ANEURYSM. DURING PLACEMENT AND REPOSITIONING OF THE 8TH COIL, THE COIL UNEXPECTEDLY DETACHED IN THE CAROTID ARTERY AND THERE WAS A TEMPORARY HICCUP FLOW. A SNARE WAS USED TO RETRIEVE THE DETACHED COIL SEGMENT. THERE WAS NO REPORTED PATIENT INJURY OR SEQUELA.

    Patient problems: No Consequences Or Impact To Patient

    MAUDE report 9760301 ↗

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.