BEUDAMED
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    32MM +4 V40 TAPER VIT HEAD

    FDA Adverse Event
    Malfunction ·STRYKER ORTHOPAEDICS CORK, STRYKER ORTHOPAEDICS·Product code KWY·February 5, 2010

    NV GXL LNR, LIPPED, 36MM ID, GROUP 3 CUPS

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JDI·July 9, 2024

    METHA SHORT HIP STEM CAP SIZE 1

    FDA Adverse Event
    Injury ·AESCULAP AG·Product code LWJ·March 16, 2021

    BIOLOX DELTA FEMORAL HEAD 32MM OD, -3.5MM

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JDI·October 3, 2024

    NV GXL LINR, NTRL, 28MM ID, GROUP 1 CUPS

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JDI·October 11, 2024

    Novation Press-Fit Tapered, Standard Offset, 12/14 Taper, Size 14, Femoral Stem, Catalog Number 160-00-14; For use in primary total hip arthroplasty.

    FDA Enforcement
    Class II ·Terminated·Exactech, Inc.·June 8, 2016

    Novation Press-Fit Tapered, Standard Offset, HA Coated, 12/14 Taper, Femoral Stem; Catalog Number 160-10-16; For use in primary total hip arthroplasty.

    FDA Enforcement
    Class II ·Terminated·Exactech, Inc.·June 8, 2016

    Novation Press-Fit Splined, Standard Offset, HA Coated, 12/14 Taper, Size 11, Femoral Stem; Catalog Number 160-30-11; For use in primary total hip arthroplasty.

    FDA Enforcement
    Class II ·Terminated·Exactech, Inc.·June 8, 2016

    Novation Press-Fit Tapered, Standard Offset, 12/14 Taper, Size 13, Femoral Stem, Catalog Number 160-00-13; For use in primary total hip arthroplasty.

    FDA Enforcement
    Class II ·Terminated·Exactech, Inc.·June 8, 2016

    NV GXL LINR, NTRL, 36MM ID, GROUP 3 CUPS

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JDI·October 28, 2024

    TRINITY

    FDA Adverse Event
    Malfunction ·CORIN MEDICAL·Product code LWJ·October 18, 2016

    TRINITY

    FDA Adverse Event
    Malfunction ·CORIN MEDICAL·Product code LWJ·December 21, 2016

    ZIMMER VERSYS FEMORAL STEM

    FDA Adverse Event
    Injury ·ZIMMER MANUFACTURING B.V.·Product code LWJ·November 21, 2016

    PROFEMUR(R) MODULAR FEMORAL NECK

    FDA Adverse Event
    Injury ·MICROPORT ORTHOPEDICS INC.·Product code LWJ·November 15, 2016

    ZIMMER M/L KINECTIV NECK

    FDA Adverse Event
    Injury ·ZIMMER, INC.·Product code LWJ·October 21, 2016

    ZMR HIP SYSTEM

    FDA Adverse Event
    Injury ·ZIMMER, INC.·Product code LWJ·December 30, 2016

    ZIMMER M/L TAPER WITH KINECTIV FEMORAL STEM

    FDA Adverse Event
    Injury ·ZIMMER, INC.·Product code LWJ·November 21, 2016

    C-TAPER COCR LFIT HEAD 26MM/+5

    FDA Adverse Event
    Malfunction ·STRYKER ORTHOPAEDICS-MAHWAH·Product code LWJ·December 14, 2016

    S-ROM STYLE FEMORAL SLEEVE

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS·Product code LWJ·December 27, 2016

    PROFEMUR(R) ROUGHENED DISTAL STEM, TAPERED

    FDA Adverse Event
    Injury ·MICROPORT ORTHOPEDICS INC.·Product code LWJ·November 28, 2016