V-Trak 7310-1230-A2Recalls & reported problems
Microvention, Inc. · HydroFill Advanced · Class 2 · Implant
All models of V-Trak (75)
Data updated Oct 16, 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 00816777023469), received between Apr 23, 2021 and Apr 23, 2021 — 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. 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 Component1
- Difficult to Remove1
- Stretched1
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.
InjuryApr 23, 2021Difficult to Remove; Stretched; Detachment of Device or Device Component; Difficult to Remove; Stretched; Detachment of Device or Device Component
IT WAS REPORTED THAT A EMBOLIZATION COIL IMPLANT WAS APPROXIMATELY 60% DEPLOYED IN AN ANEURYSM OF THE INTERNAL CAROTID ARTERY TERMINUS WHEN IT BEGAN TO STRETCH. THE PHYSICIAN ATTEMPTED TO WITHDRAW THE COIL AND THE PUSHER WIRE DETACHED. THE MICROCATHETER WAS REMOVED AND THE STRETCHED COIL WAS LEFT IN THE PATIENT. THE COIL STRETCHED DOWN TO THE PATIENT'S GROIN. THE PATIENT WAS REPORTED TO BE "OK." THERE WAS NO REPORTED INTERVENTION OR INJURY TO THE PATIENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 11713556 ↗
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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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