About NeuroAlert

NeuroAlert is an independent, informational dashboard that consolidates publicly available post-market safety data for neurovascular (neurointerventional) medical devices — such as embolization coils, flow diverters, thrombectomy catheters, and intracranial stents — into a single, continuously updated view.

The project was created by a practicing interventional neuroradiologist to make scattered, multi-language regulatory data easier to monitor. Recall and adverse-event information for these devices is published by different national regulators in different formats and languages, which makes cross-border awareness difficult. NeuroAlert gathers these signals into one place.

What this site does

• Aggregates device recall and adverse-event records from the U.S. FDA (openFDA), Korea's MFDS, and Japan's PMDA.
• Filters records to a curated whitelist of neurovascular device categories, so unrelated products are excluded.
• Sends optional email alerts when a new US or Korean recall matching that whitelist is detected.

Who maintains it

NeuroAlert is maintained by an individual clinician, not by any regulatory agency, manufacturer, or commercial sponsor. The underlying data belongs to the respective regulatory agencies and is used here for informational aggregation only. For questions, corrections, or collaboration, please use our contact page.