BEUDAMED
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    Filters FDA Adverse Event ×

    JUVEDERM ULTRA XC/LIDO (VOLUME UNKNOWN)

    FDA Adverse Event
    Injury ·PRINGY·Product code LMH·November 22, 2024

    FKX

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·July 29, 2016

    *

    FDA Adverse Event
    Malfunction ·3M COMPANY·Product code EBI·October 6, 2006

    2.0MM QFX SCREW 18MM

    FDA Adverse Event
    Malfunction ·SMITH & NEPHEW, INC.·Product code HRS·May 13, 2021

    2.0MM QFX SCREW 12MM

    FDA Adverse Event
    Malfunction ·SMITH & NEPHEW, INC.·Product code HRS·August 5, 2025

    TECNIS SYMFONY TORIC

    FDA Adverse Event
    Injury ·JOHNSON & JOHNSON SURGICAL VISION, INC.·Product code POE·June 5, 2018

    FOREARM CRUTCHES

    FDA Adverse Event
    Injury ·KX MEDICAL·Product code IPR·May 7, 2018

    FKX SYSTEM, PERITONEAL, AUTOMATIC DELIVERY

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FKX·May 22, 2014

    NSK

    FDA Adverse Event
    Malfunction ·NAKANISHI INC.·Product code ELC·August 23, 2021

    Q50 PLUS STENT GRAFT BALLOON CATHETER

    FDA Adverse Event
    Death ·QX MEDICAL, LLC·Product code MJN·December 28, 2016

    FULL CUFF FOREARM CRUTCH

    FDA Adverse Event
    Injury ·KX MEDICAL LLC·Product code IPR·December 20, 2023

    FULL CUFF FOREARM CRUTCH

    FDA Adverse Event
    Injury ·KX MEDICAL LLC.·Product code IPR·December 20, 2023

    5002-KX-B

    FDA Adverse Event
    Malfunction ·WELCH ALLYN, INC.·Product code FRI·December 2, 2025

    KX+FEM IMPACTOR

    FDA Adverse Event
    Malfunction ·HOWMEDICA INC.·Product code HWA·July 7, 1997

    KX+ FEM IMPACTOR

    FDA Adverse Event
    Malfunction ·HOWMEDICA·Product code HWA·May 8, 1997

    KX+ FEM IMPACTOR

    FDA Adverse Event
    Malfunction ·HOWMEDICA INC.·Product code HWA·August 7, 1998

    KX+ FEM IMPACTOR

    FDA Adverse Event
    Malfunction ·HOWMEDICA INC.·Product code HWA·December 16, 1998

    KX+ FEM IMPACTOR

    FDA Adverse Event
    Malfunction ·HOWMEDICA INC·Product code HWA·October 1, 1998

    KX+FEM IMPACTOR

    FDA Adverse Event
    Malfunction ·HOWMEDICA INC.·Product code HWA·October 6, 1998

    KX+ FEM IMPACTOR

    FDA Adverse Event
    Malfunction ·HOWMEDICA INC.·Product code HWA·October 8, 1998