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    EXETER V40 STEM 37.5MM NO1L125

    FDA Adverse Event
    Malfunction ·STRYKER ORTHOPAEDICS-MAHWAH·Product code JDI·July 13, 2017

    EXETER V40 STEM 37.5MM NO 3

    FDA Adverse Event
    Malfunction ·STRYKER ORTHOPAEDICS-MAHWAH·Product code LPH·May 31, 2017

    EXETER V40 STEM 35.5MM

    FDA Adverse Event
    Malfunction ·STRYKER ORTHOPAEDICS-MAHWAH·Product code LPH·July 12, 2017

    EXETER V40 STEM 44MM NO 0

    FDA Adverse Event
    Malfunction ·STRYKER ORTHOPAEDICS-MAHWAH·Product code LPH·October 24, 2017

    EXETER V40 STEM 44MM NO 2

    FDA Adverse Event
    Malfunction ·STRYKER ORTHOPAEDICS-MAHWAH·Product code JDI·November 26, 2014

    DEDICACE. V40(TM) FEMORAL STEM

    FDA Adverse Event
    Malfunction ·STRYKER ORTHOPAEDICS-MAHWAH·Product code LPH·November 21, 2016

    ETS. HIP ENDOPROSTHESIS

    FDA Adverse Event
    Malfunction ·STRYKER ORTHOPAEDICS-MAHWAH·Product code LPH·July 20, 2015

    EXETER V40 STEM 44MM NO 4

    FDA Adverse Event
    Malfunction ·STRYKER ORTHOPAEDICS-MAHWAH·Product code JDI·December 22, 2020

    EXETER V40 STEM 50MM NO 1

    FDA Adverse Event
    Malfunction ·STRYKER ORTHOPAEDICS-MAHWAH·Product code JDI·May 6, 2019

    DEDICACE. V40(TM) FEMORAL STEM

    FDA Adverse Event
    Malfunction ·STRYKER ORTHOPAEDICS-MAHWAH·Product code LZO·January 11, 2016

    X-CHANGE III CONNECTOR

    FDA Adverse Event
    Malfunction ·STRYKER ORTHOPAEDICS-MAHWAH·Product code LXH·February 26, 2015

    RESTORATION(TM) ADM. PRESS

    FDA Adverse Event
    Malfunction ·STRYKER ORTHOPAEDICS-MAHWAH·Product code LPH·July 1, 2016

    EXETER V40 STEM 44MM NO 4

    FDA Adverse Event
    Malfunction ·STRYKER ORTHOPAEDICS-MAHWAH·Product code LPH·January 19, 2021

    EXETER V40 STEM 37.5MM NO 4

    FDA Adverse Event
    Malfunction ·STRYKER ORTHOPAEDICS-MAHWAH·Product code LPH·January 19, 2021

    EXETER V40 STEM 44MM NO 4

    FDA Adverse Event
    Malfunction ·STRYKER ORTHOPAEDICS-MAHWAH·Product code LPH·January 19, 2021

    PATELLAR TENDON HEMI

    FDA Adverse Event
    Malfunction ·REGENERATION TECHNOLOGIES·Product code LMO·February 26, 2004

    ALLOWASH

    FDA Adverse Event
    Malfunction ·COMMUNITY BLOOD CTR AND TISSUE SVS·Product code LMO·February 7, 2002

    PRE-SHAPED ACHILLES TENDON W/CALCANEUS

    FDA Adverse Event
    Malfunction ·REGENERATION TECHNOLOGIES, INC.·Product code LMO·August 26, 2003

    BONE DOWEL - IRRADIATED 1.4CM

    FDA Adverse Event
    Malfunction ·MICHIGAN TISSUE BANK·Product code LMO·May 17, 1993

    CLOWARD DOWEL - IRRADIATED 1.4 X 2.4CM

    FDA Adverse Event
    Malfunction ·DAYTON REGIONAL TISSUE BANK·Product code LMO·May 17, 1993