BEUDAMED
    6 results · 63ms · Sources: EU EUDAMED, US FDA

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    THROMBECTOMY DEVICE

    FDA Adverse Event
    Malfunction ·INARI MEDICAL - OAK CANYON·Product code DXE·December 17, 2021

    FLOW TRIEVER INARI MEDICAL

    FDA Adverse Event
    Death ·INARI MEDICAL - OAK CANYON·Product code DXE·November 8, 2021

    ClotTriever XL Catheter, 30 mm, REF: 41-102, used with Instructions for Use ClotTriever XL Catheter ClotTriever Thrombectomy System, Reference: IU-01011

    FDA Recall
    Open, Classified ·Inari Medical Oak Canyon·Product code QEW·July 19, 2024

    Artix MT Thrombectomy Device, REF: 32-102

    FDA Recall
    Open, Classified ·Inari Medical Oak Canyon·Product code QEW·April 8, 2025

    Artix MT Thrombectomy Device, REF: 32-102

    FDA Enforcement
    Class II ·Ongoing·Inari Medical - Oak Canyon·May 14, 2025

    ClotTriever XL Catheter, 30 mm, REF: 41-102, used with Instructions for Use ClotTriever XL Catheter ClotTriever Thrombectomy System, Reference: IU-01011

    FDA Enforcement
    Class I ·Ongoing·Inari Medical - Oak Canyon·August 28, 2024