BEUDAMED
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    Filters Status: Malfunction ×

    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

    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

    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

    KX+ FEM IMPACTOR

    FDA Adverse Event
    Malfunction ·HOWMEDICA INC.·Product code HWA·October 12, 1998

    KX+FEM IMPACTOR

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

    KX+ DURATION PATELLA MED

    FDA Adverse Event
    Malfunction ·HOWMEDICA INC·Product code HTG·November 25, 1998

    KX+ DURAT STAB INSERT 12MM

    FDA Adverse Event
    Malfunction ·STRYKER ORTHOPAEDICS LIMERICK·Product code HSX·January 25, 2011

    KX PLUS FEM CONDY NONPOR XLG

    FDA Adverse Event
    Malfunction ·HOWMEDICA INC.·Product code HSA·August 27, 1998

    KX PLUS FEM CONDY NONPOR XLG

    FDA Adverse Event
    Malfunction ·HOWMEDICA INC.·Product code HSA·July 14, 1998