BEUDAMED
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    DEPUY ORTHOPAEDICS, INC.

    FDA Adverse Event
    Injury ·DEPUY ORTHOPADICS, INC.·Product code JWH·December 23, 2004

    DEPUY ORTHOPAEDICS, INC

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code KWY·March 27, 2009

    SIG MOD TIB TRAY CEM COCR 4

    FDA Adverse Event
    Injury ·1818910 DEPUY ORTHOPAEDICS, INC.·Product code LPH·September 22, 2014

    SROM MARATHON LINER M 28 NEU

    FDA Adverse Event
    Injury ·1818910 DEPUY ORTHOPAEDICS, INC.·Product code LPH·December 2, 2015

    UNKNOWN DEPUY AML CUP

    FDA Adverse Event
    Injury ·1818910 DEPUY ORTHOPAEDICS, INC.·Product code KWA·October 6, 2014

    PINNACLE 300 ACET CUP 52MM

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC. 1818910·Product code LPH·May 2, 2013

    UNK HIP FEMORAL STEM CORAIL

    FDA Adverse Event
    Injury ·DEPUY IRELAND - 9616671·Product code LZO·November 13, 2024

    UNK KNEE FEMORAL SIGMA

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code JWH·September 13, 2022

    UNK KNEE FEMORAL SIGMA

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code JWH·September 13, 2022

    UNK KNEE PATELLA SIGMA

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS INC US·Product code JWH·September 13, 2022

    5.5MM POLYAXIAL SCREW FT 25MM

    FDA Adverse Event
    Injury ·BIOMET·Product code HRS·February 18, 2013

    LINEAGE(R) TRANSCEND(R) CERAMIC FEMORAL HEAD

    FDA Adverse Event
    Injury ·WRIGHT MEDICAL TECHNOLOGY, INC.·Product code LPH·October 2, 2013

    LINEAGE(R) TRANSCEND(R) CERAMIC ACETABULAR LINER

    FDA Adverse Event
    Injury ·WRIGHT MEDICAL TECHNOLOGY, INC.·Product code MRA·October 2, 2013

    TRANSCEND(R) QUADRANT SHELL

    FDA Adverse Event
    Injury ·WRIGHT MEDICAL TECHNOLOGY, INC.·Product code LPH·October 2, 2013

    ORTHOSORB 1 PIN 50X1.3MM KIT

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code OVZ·June 4, 2013

    UNKNOWN AFFIXUS ANTI-ROTATION SCREW

    FDA Adverse Event
    Injury ·BIOMET·Product code HRS·October 17, 2012

    UNKNOWN AFFIXUS LAG SCREW

    FDA Adverse Event
    Injury ·BIOMET·Product code HSB·October 17, 2012

    LAG SCREW DRILL

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code LXH·September 20, 2013

    S-ROM*HEAD FEMORAL COCR 28+0

    FDA Adverse Event
    Injury ·8010379 DEPUY INTL., LTD·Product code JDI·December 3, 2015

    S-ROM*SCREW,5.0MM DIA,35 MM LG

    FDA Adverse Event
    Injury ·1219655 DEPUY-RAYNHAM·Product code LPH·December 3, 2015