BEUDAMED
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    Filters Status: Injury ×

    NEXGEN ALL POLY PATELLA

    FDA Adverse Event
    Injury ·ZIMMER MANUFACTURING B.V.·Product code JWH·September 7, 2018

    NEXGEN ARTICULAR SURFACE

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·September 7, 2018

    NEXGEN STEMMED TIBIAL COMPONENT

    FDA Adverse Event
    Injury ·ZIMMER MANUFACTURING B.V.·Product code JWH·September 7, 2018

    NEXGEN CR-FLEX FEMORAL COMPONENT

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code MBH·September 7, 2018

    CYPHER SIROLIMUS-ELUTING CORONARY STENT

    FDA Adverse Event
    Injury ·CORDIS DE MEXICO·Product code NIQ·August 10, 2007

    ALINITY I STAT HIGH SENSITIVE TROPONIN-I REAGENT KIT

    FDA Adverse Event
    Injury ·A.I.D.D LONGFORD·Product code MMI·June 20, 2022

    SYNCHROMED II

    FDA Adverse Event
    Injury ·MDT PUERTO RICO OPERATIONS CO·Product code LKK·November 18, 2013

    CYPHER SIROLIMUS-ELUTING CORONARY STENT

    FDA Adverse Event
    Injury ·CORDIS EUROPA, N.V.·Product code NIQ·September 17, 2003

    CYPHER SIROLIMUS-ELUTING CORONARY STENT

    FDA Adverse Event
    Injury ·CORDIS DE MEXICO·Product code NIQ·June 6, 2007

    TMAX

    FDA Adverse Event
    Injury ·OKLAHOMA CITY MANUFACTURING SITE·Product code FWZ·July 17, 2014

    TMAX

    FDA Adverse Event
    Injury ·OKLAHOMA CITY MANUFACTURING SITE·Product code FWZ·July 18, 2014

    TMAX

    FDA Adverse Event
    Injury ·OKLAHOMA CITY MANUFACTURING SITE·Product code FWZ·July 18, 2014

    SYNCHROMED II

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code LKK·July 2, 2010

    TAXUS EXPRESS2 PACLITAXEL-ELUTING STENT

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORP.·Product code NIQ·September 14, 2006

    CONSERVE(R) TOTAL A-CLASS HEAD

    FDA Adverse Event
    Injury ·MICROPORT ORTHOPEDICS INC.·Product code JDL·March 23, 2016

    PULSE GEN MODEL 106

    FDA Adverse Event
    Injury ·LIVANOVA USA, INC.·Product code LYJ·August 18, 2017

    TAXUS EXPRESS2 PACLITAXEL-ELUTING STENT

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORP.·Product code NIQ·September 14, 2006

    UNKNOWN-CPK-NG TUBE

    FDA Adverse Event
    Injury ·HALYARD HEALTH·Product code KNT·July 11, 2018

    DH CPK NG TUBES

    FDA Adverse Event
    Injury ·HALYARD HEALTH·Product code KNT·June 22, 2018

    CROSSSAIL CORONARY DILATATION CATHETER

    FDA Adverse Event
    Injury ·GUIDANT VASCULAR INTERVENTION·Product code LOX·November 3, 2004