BEUDAMED
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    XIENCE V EVEROLIMUS ELUTING CORONARY STENT SYSTEM

    FDA Adverse Event
    Malfunction ·AV-TEMECULA-CT·Product code NIQ·August 23, 2011

    ENDOTAK RELIANCE

    FDA Adverse Event
    Injury ·CPI - DEL CARIBE·Product code NVY·November 3, 2014

    PELVICOL ACELLULAR COLLAGEN MATRIX 4X7CM

    FDA Adverse Event
    Injury ·COVIDIEN, FORMERLY TISSUE·Product code FTL·July 3, 2013

    UNKNOWN FEMORAL HEAD

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code JDI·March 16, 2017

    CER BIOLOXD OPTION HD 36MM

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code LZO·May 12, 2022

    G7 HI-WALL E1 LINER 36MM H

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code PBI·March 16, 2017

    G7 HI-WALL E1 LINER 36MM H

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code PBI·March 16, 2017

    M2A-MAGNUM MOD HD SZ 50MM

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·July 16, 2015

    M2A-MAGNUM PF CUP 56ODX50ID

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·July 16, 2015

    SELEX/MAGNUM MOD HD 40MM +6

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code LZO·July 16, 2015