BEUDAMED
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    COCR HEAD

    FDA Adverse Event
    Injury ·MICROPORT ORTHOPEDICS INC.·Product code LZO·March 25, 2026

    COCR HEAD

    FDA Adverse Event
    Injury ·MICROPORT ORTHOPEDICS INC.·Product code LZO·March 30, 2026

    CUPULE MOBILE A BAGUE

    FDA Adverse Event
    Injury ·MICROPORT ORTHOPEDICS INC.·Product code LZO·March 25, 2026

    CUPULE MOBILE A BAGUE

    FDA Adverse Event
    Injury ·MICROPORT ORTHOPEDICS INC.·Product code LZO·March 30, 2026

    CUPULE MOBILE A BAGUE

    FDA Adverse Event
    Injury ·MICROPORT ORTHOPEDICS INC.·Product code LZO·March 30, 2026

    HOC PLUS ENDOTOUCH APPL 13" CVD

    FDA Adverse Event
    Malfunction ·TELEFLEX MEDICAL·Product code GEF·July 13, 2015

    HOC PLUS ENDOTOUCH APPLIER 13" CVD

    FDA Adverse Event
    Malfunction ·TELEFLEX·Product code GDO·February 26, 2014

    HOC PLUS ENDOTOUCH APPLIER 13" CVD

    FDA Adverse Event
    Malfunction ·TELEFLEX·Product code GDO·August 22, 2012

    HOC PLUS ENDOTOUCH APPLIER 13" CVD

    FDA Adverse Event
    Malfunction ·TELEFLEX·Product code GDO·August 22, 2012

    HOC PLUS ENDOTOUCH APPLIER 13" CURVED

    FDA Adverse Event
    Malfunction ·TELEFLEX·Product code FZP·October 24, 2013

    LIFECARE IV PUMP

    FDA Adverse Event
    Injury ·ABBOTT LABORATORIES·Product code FRN·June 13, 1995

    MONACO RTP SYSTEM

    FDA Adverse Event
    Malfunction ·IMPAC MEDICAL SYSTEMS, INC·Product code MUJ·February 20, 2014

    4D INTEGRATED TREATMENT CONSOLE

    FDA Adverse Event
    VARIAN MEDICAL SYSTEMS, INC·Product code IYE·February 16, 2012

    UNKNOWN ULTRABUTTON DEV

    FDA Adverse Event
    Injury ·ARTHROCARE CORPORATION·Product code MBI·January 11, 2023

    UNKNOWN ULTRABUTTON DEV

    FDA Adverse Event
    Injury ·ARTHROCARE CORPORATION·Product code MBI·January 9, 2023

    UNKNOWN PEEK INTERFERENCE SCREW

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC.·Product code MAI·January 9, 2023

    UNKNOWN ULTRABUTTON DEV

    FDA Adverse Event
    Injury ·ARTHROCARE CORPORATION·Product code MBI·January 11, 2023

    MOSAIQ

    FDA Adverse Event
    Malfunction ·IMPAC MEDICAL SYSTEMS, INC.·Product code IYE·August 26, 2016

    UNKNOWN PEEK INTERFERENCE SCREW

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC.·Product code MBI·January 10, 2023

    UNKNOWN BIOABSORBABLE BIORCI AND GTS INTERFERENCE SCREW

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC.·Product code MBI·January 10, 2023