GORE VIABAHN VBX Balloon Expandable EndoRecalls & reported problems across all models
W. L. Gore & Associates, Inc. · 111 models in the FDA device registry
Data updated Oct 18, 2026 from official FDA records · Editorial policy
GORE VIABAHN VBX Balloon Expandable Endo models — page 2
111 models, 100 per page, most reported first. Each model has its own page with its reports, recalls and device details.
- GORE VIABAHN VBX Balloon Expandable Endo BXA062901AIliac Covered Stent, Arterial2 reports
- GORE VIABAHN VBX Balloon Expandable Endo BXA102902AIliac Covered Stent, Arterial2 reports
- GORE VIABAHN VBX Balloon Expandable Endo BXA051902AIliac Covered Stent, Arterial1 report
- GORE VIABAHN VBX Balloon Expandable Endo BXA053902AIliac Covered Stent, Arterial1 report
- GORE VIABAHN VBX Balloon Expandable Endo BXA063901AIliac Covered Stent, Arterial1 report
- GORE VIABAHN VBX Balloon Expandable Endo BXA071901AIliac Covered Stent, Arterial1 report
- GORE VIABAHN VBX Balloon Expandable Endo BXA073901AIliac Covered Stent, Arterial1 report
- GORE VIABAHN VBX Balloon Expandable Endo BXA103901AIliac Covered Stent, Arterial1 report
- GORE VIABAHN VBX Balloon Expandable Endo BXA103902AIliac Covered Stent, Arterial1 report
- GORE VIABAHN VBX Balloon Expandable Endo BXA097901AIliac Covered Stent, Arterial1 report
- GORE VIABAHN VBX Balloon Expandable Endo BXA113901AIliac Covered Stent, Arterial1 report
Sources and updates
- Models: FDA GUDID, file dated Oct 13, 2026. Models are grouped by the brand name the manufacturer registered.
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026
- 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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