BEUDAMED
    9 results · 26ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    LEAD MODEL 304

    FDA Adverse Event
    Malfunction ·LIVANOVA USA, INC.·Product code LYJ·August 10, 2021

    BIPOL LEAD MODEL 300

    FDA Adverse Event
    Malfunction ·LIVANOVA USA, INC.·Product code LYJ·June 3, 2021

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·April 23, 2013

    ADVANTAGE SERIES 26

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL·Product code FPO·April 21, 2011

    SPRINT FIDELIS

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO, INC.·Product code LWS·July 10, 2008

    LEAD MODEL 304

    FDA Adverse Event
    Malfunction ·LIVANOVA USA, INC.·Product code LYJ·December 7, 2023

    LEAD MODEL 304

    FDA Adverse Event
    Malfunction ·LIVANOVA USA, INC.·Product code LYJ·January 12, 2024

    STRATA®

    FDA Adverse Event
    Malfunction ·MEDTRONIC DOMINICANA·Product code JXG·April 6, 2026

    STRATA®

    FDA Adverse Event
    Injury ·MEDTRONIC DOMINICANA·Product code JXG·April 6, 2026