BEUDAMED
    75 results · 34ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    BIOLOX DELTA OPTION CERAMIC HEADS

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code LZO·May 1, 2017

    BIOLOX DELTA OPTION CERAMIC HEADS

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code LZO·May 1, 2017

    M2A MAGNUM SYSTEM

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·May 1, 2017

    G7 DUAL MOBILITY SYSTEM, ACTIVE ARTICULATION SYSTEM

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code LPH·May 1, 2017

    M2A-T UNIV 2-HOLE SHL SZ 41/58

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWY·May 1, 2018

    32MM M2A MOD HEAD STD NK

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWA·November 15, 2017

    M2A MAGNUM SYSTEM

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·April 6, 2017

    INSPIRE 7F M N/S

    FDA Adverse Event
    Malfunction ·SORIN GROUP ITALIA·Product code DTZ·December 29, 2025

    M2A-TAPER LINER SZ 41/32

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWA·May 1, 2018

    STAPLE, IMPLANTABLE

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code GDW·May 9, 2013

    PERCLOSE PROGLIDE 6F SUTURE MEDIATED CLOSURE (SMC) SYSTEM

    FDA Adverse Event
    Injury ·AV-TEMECULA-CT·Product code MGB·May 25, 2011

    PUMP MMT-522NAS PRDGM INS V2.2 SK EN

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO OPERATIONS MED-REL·Product code LZG·August 8, 2008

    MODULAR POROUS LATERALIZED REDUCED DISTAL TAPERLOC FEMORAL STEM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code LPH·October 5, 2017

    UNKNOWN E1 LINER

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JDG·August 9, 2018

    UNKNOWN BIOLOX DELTA CERAMIC HEAD

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code MEH·August 9, 2018

    MALLORY HEAD RINGLOC RADIAL ACETABULAR CUP

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JDI·August 9, 2018

    INSPIRE 7F M N/S

    FDA Adverse Event
    Malfunction ·SORIN GROUP ITALIA - S.R.L.·Product code DTZ·February 19, 2026

    M2A-MAGNUM 42-50 TPR INSRT STD 0/0MMT1

    FDA Adverse Event
    Malfunction ·ZIMMER BIOMET, INC.·Product code KWA·November 26, 2018

    M2A-MAGNUM 52-60MM TPR INSRT-6

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWA·June 28, 2019

    M2A-MAGNUM MOD HD SZ 52MM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JDI·March 26, 2018