VIA Microcatheter VIA-17-154-90-MVI2Recalls & reported problems
Microvention, Inc. · VIA 17 Microcatheter · Class 2
All models of VIA Microcatheter (10)
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 00842429106457), received between Apr 28, 2022 and Apr 28, 2022 — 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
- Material Separation1
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.
MalfunctionApr 28, 2022Material Separation; Detachment of Device or Device Component; Material Separation; Detachment of Device or Device Component
IT WAS REPORTED THAT AFTER THE WEB DEVICE WAS DELIVERED USING THE VIA 17 THROUGH A SOFIA 6F 125CM AND SYNCHRO 14 WIRE, THE PHYSICIAN PULLED THE VIA 17 CATHETER OUT AND THE END OF THE CATHETER DETACHED. THERE WAS NO REPORTED PATIENT INJURY AND THE PATIENT WAS REPORTED TO BE DOING FINE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 14246817 ↗
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- WATCHMAN™ TruSeal™ Access System M635TU70020Boston Scientific Corporation · Catheter, percutaneous1 recall11 deaths217 reports
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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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