V-Trak 100830HCSR-R-V-A2Recalls & reported problems
Microvention, Inc. · MicroPlex Helical Regular · Class 2 · Implant
All models of V-Trak (75)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- 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 00816777020451), received between Jan 17, 2020 and Jan 17, 2020 — classified as 1 malfunction.
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. 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 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.
MalfunctionJan 17, 2020Detachment of Device or Device Component; Detachment of Device or Device Component
IT WAS REPORTED THAT AN EMBOLIZATION COIL UNEXPECTEDLY DETACHED WHILE PARTIALLY DEPLOYED IN THE VESSEL. THE COIL COULD NOT BE RETRACTED BACK INTO THE MICROCATHETER. THE PUSHER AND MICROCATHETER WERE REMOVED; HOWEVER, THE IMPLANT COIL WAS LEFT IN A MORE PROXIMAL SEGMENT OF THE VESSEL. THERE WAS NO REPORTED INTERVENTION OR PATIENT INJURY. THE PATIENT WAS REPORTED TO HAVE LEFT THE HOSPITAL ONE DAY AFTER THE PROCEDURE IS GOOD CONDITION.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 9604641 ↗
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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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