PIPELINERecalls & reported problems across all models
Micro Therapeutics, Inc. · 114 models in the FDA device registry
Data updated Oct 18, 2026 from official FDA records · Editorial policy
PIPELINE models — page 2
114 models, 100 per page, most reported first. Each model has its own page with its reports, recalls and device details.
- Pipeline PED-475-35Intracranial aneurysm flow diverter2 reports
- PIPELINE PED-375-18Intracranial aneurysm flow diverter2 reports
- Pipeline PED-400-18Intracranial aneurysm flow diverter1 report
- Pipeline PED-400-20Intracranial aneurysm flow diverter1 report
- Pipeline PED-425-16Intracranial aneurysm flow diverter1 report
- Pipeline PED-425-18Intracranial aneurysm flow diverter1 report
- Pipeline PED-450-18Intracranial aneurysm flow diverter1 report
- Pipeline PED-500-16Intracranial aneurysm flow diverter1 report
- Pipeline PED-500-20Intracranial aneurysm flow diverter1 report
- Pipeline PED-350-35Intracranial aneurysm flow diverter1 report
- Pipeline PED-400-25Intracranial aneurysm flow diverter1 report
- Pipeline PED-400-35Intracranial aneurysm flow diverter1 report
- Pipeline PED-500-35Intracranial aneurysm flow diverter1 report
- PIPELINE PED-350-14Intracranial aneurysm flow diverter1 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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