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MicroPlex Helical Soft 100408HCSR-S-VRecalls & reported problems

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

All models of MicroPlex Helical Soft (9)

Data updated Oct 16, 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 00811425025017), received between Jul 11, 2018 and Jul 11, 2018 — 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 16, 2026.

Most reported problems

Device problems

  • Detachment of Device or Device Component1
  • Stretched1

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.

  • MalfunctionJul 11, 2018Stretched; Detachment of Device or Device Component; Stretched; Detachment of Device or Device Component

    IT WAS REPORTED THAT AN EMBOLIZATION COIL STRETCHED DURING REMODELING WITH A BALLOON. THE COIL DETACHED INSIDE THE MICROCATHETER. BOTH SEGMENTS WERE REMOVED IN THEIR ENTIRETY FROM THE PATIENT. THERE WAS NO REPORTED INTERVENTION OR PATIENT INJURY.

    Patient problems: No Consequences Or Impact To Patient

    MAUDE report 7677789 ↗

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Sources and updates

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