BEUDAMED
    10,000 results · 86ms · Sources: EU EUDAMED, US FDA

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    UNKNOWN BI-METRIC COLLARLESS STEM

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code KWA·November 23, 2017

    UNKNOWN BI-METRIC COLLARLESS STEM

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code JDI·November 23, 2017

    UNKNOWN BIMETRIC (TITANIUM) STEM

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code JDI·November 22, 2017

    UNKNOWN FEMORAL HEAD

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code JDI·November 22, 2017

    OXF UNI TIB TRAY SZ C RM PMA

    FDA Adverse Event
    Malfunction ·BIOMET UK LTD.·Product code NRA·May 10, 2018

    OXF TWIN-PEG CMNTD FEM SM PMA

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code NRA·March 27, 2019

    OXF ANAT BRG RT SM SIZE 3 PMA

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code NRA·March 27, 2019

    OXF UNI SILICONE ANKLE STRAP

    FDA Adverse Event
    Malfunction ·BIOMET UK LTD.·Product code HRY·February 20, 2018

    OXF UNI TIB TRAY SZA RM/LL PMA

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code NRA·March 27, 2019

    Biomet Vanguard(TM) DCM PS Plus 16mm x 63/67mm Tibial Bearing (REF. 183726), ARCOM UHMWPE, sterile, Biomet Orthopedics, Inc., Warsaw, IN. A knee prosthesis intended for single use implantation to replace the articular portions of the knee joint.

    FDA Recall
    Terminated ·Biomet, Inc.·Product code JWH·September 22, 2008

    OXF UNI TIB TRAY SZ B LM PMA

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code NRA·November 16, 2017

    OXF ANAT BRG RT LG SIZE 3 PMA

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code NRA·May 7, 2025

    MODULAR FINNED STEM

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS, LLC·Product code JWH·March 27, 2012

    M2A 38MM MOD HD +3MM NK

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS LLC·Product code KWA·November 11, 2017

    M2A-38 CUP NON FLARED SZ 62MM

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS LLC.·Product code KWA·November 11, 2017

    MODULAR REAMER HEAD

    FDA Adverse Event
    Malfunction ·BIOMET ORTHOPEDICS, LLC·Product code HTO·May 5, 2021

    CALIBRATED DRILL BIT

    FDA Adverse Event
    Malfunction ·BIOMET ORTHOPEDICS, LLC·Product code HTW·June 21, 2021

    TAPERLOC COMPLETE PRIMARY FEMORAL

    FDA Adverse Event
    Malfunction ·BIOMET ORTHOPEDICS, LLC·Product code KWL·August 10, 2021

    JUGGERKNOT SOFT ANCHORS

    FDA Adverse Event
    Malfunction ·BIOMET ORTHOPEDICS, LLC·Product code MBI·September 30, 2024

    TI LOW PROFILE SCREW 6.5X25MM

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS LLC·Product code LPH·December 13, 2017