Cosmos 18 Advanced 8218-1347Recalls & reported problems
Microvention, Inc. · V-Trak · Class 2 · Implant
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- 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 00811425028797), received between Aug 26, 2016 and Aug 26, 2016 — classified as 1 injury.
The most frequently reported specific device problem is “Detachment Of 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. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.
Most reported problems
Device problems
- Detachment Of Device Component1
- Device Issue1
Patient problems
- Aneurysm1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryAug 26, 2016Detachment Of Device Component; Device Issue; Detachment Of Device Component; Device Issue
IT WAS REPORTED THAT DURING THE EMBOLIZATION TREATMENT OF AN AVM OFF A VERTEBRAL FEEDER ARTERY, THE EMBOLIZATION COIL WAS POSITIONED IN THE FEEDER ARTERY. AFTER 50% OF THE COIL WAS POSITIONED, THE COIL PREMATURELY DETACHED WITHIN THE ARTERY. THE REMAINING COIL (OUTSIDE OF THE INTENDED LOCATION) WAS TACKED IN PLACE USING 2 WINGSPAN STENTS TO KEEP THE COIL INTACT AGAINST THE VESSEL WALL SUCCESSFULLY. THE PATIENT WAS REPORTED TO BE OKAY.
Patient problems: Aneurysm
MAUDE report 5907017 ↗
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Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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