NeuroAlert — Global Neurovascular Device Safety Monitor

Recent Recall & Safety Events

Most recent regulatory actions matching the neurovascular device whitelist.

Date range → 제외된 항목 보기

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Source	Manufacturer	Device	Category	Date

US Recalls + adverse events, auto-updated.
KR Recall/withdrawal items only. No public adverse-event or detailed-reason data; product names are class-level.
AU Device recalls with manufacturer, product, reason, hazard class, and date.
CA Device recalls with product, issue, recall class, and date.
JP Device recalls with product, manufacturer, reason, and date (translated from Japanese).
DE Manufacturer field safety notices (translated from German); reason from official PDF.
UK Field safety notices with manufacturer, device, reason, and action (from FSN PDF).
CH Field safety corrective actions with manufacturer, device, and date; reason extracted from official FSN PDF.
FR Safety information (recalls, user information) with manufacturer, device, and date; reason extracted from official FSN PDF (translated from French).
US FDA Alerts: curated most-serious recalls & early alerts with images (CDRH).

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