Reporting adverse incidents: inferior vena cava filter (IVC)

IVCs (Intra-Venous Cannulae) adverse incident reports should follow established guidelines, specifically MEDDEV 2.12/1 for medical devices vigilance systems. Reports must include details such as product identification, description of incident, and patient harm or outcome. Incident classification, investigation, and reporting timelines are also critical components. A designated contact person or department is usually responsible for managing these reports.