MicroPlex Cosmos 181347CS-VRecalls & reported problems
Microvention, Inc. · V-Trak · Class 2 · Implant
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00810170014116), received between Nov 21, 2020 and Nov 12, 2021 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Detachment of Device or Device Component” (2 reports).
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 16, 2026.
Most reported problems
Device problems
- Detachment of Device or Device Component2
Patient problems
- No Clinical Signs, Symptoms or Conditions2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionNov 12, 2021Detachment of Device or Device Component; Detachment of Device or Device Component
IT WAS REPORTED THAT DURING AN EMBOLIZATION TREATMENT OF A BASILAR ANEURYSM, THE SECOND COIL BECAME STUCK WITHIN THE MICROCATHETER. UPON WITHDRAW THE COIL DETACHED FROM THE DELIVERY PUSHER WITHIN THE MICROCATHETER. THE COIL AND MICROCATHETER WERE WITHDRAWN TOGETHER AND THE PROCEDURE WAS COMPLETED SUCCESSFULLY. NO PATIENT HARM OR INJURY WAS REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 12807831 ↗MalfunctionNov 21, 2020Detachment of Device or Device Component; Detachment of Device or Device Component
IT WAS REPORTED THAT DURING A COIL EMBOLIZATION PROCEDURE, THE EMBOLIZATION COIL STRETCHED AND DETACHED INSIDE THE MICROCATHETER. THE COIL WAS REMOVED FROM THE PATIENT. THERE WAS NO REPORTED PATIENT INJURY OR ADDITIONAL INTERVENTION. THE PATIENT IS CURRENTLY REPORTED TO BE DOING "GREAT."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 10880877 ↗
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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 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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