BEUDAMED
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    COMPREHENSIVE LOCKING SCREW

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code HWC·July 5, 2019

    COMP RVRS 25MM BSPLT HA+ADPTR

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWS·March 8, 2021

    0.7/1.2JG326D-265 Product Usage: The device is a mobile X-ray system in order to take general radiography of patients in the hospital who cannot move and/or of outpatients in emergency.

    FDA Enforcement
    Class II ·Terminated·Shimadzu Medical Systems·November 14, 2012

    SPECIFIC DEVICE NOT REPORTED

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code KWT·July 7, 2025

    XTND 145 RSA REAM GUID INSRTR

    FDA Adverse Event
    Malfunction ·DEPUY IRELAND - 9616671·Product code PHX·June 5, 2023

    145-DEG PE 36MM HUM LINER +0

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code KWS·December 10, 2024

    EQUINOXE ANATOMIC SHOULDER COMPONENTS

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code KWS·May 22, 2025

    UNKNOWN PERFORM REVERSED ECCENTRIC GLENOSPHERES

    FDA Adverse Event
    Malfunction ·TORNIER S.A.S.·Product code KWS·September 12, 2022

    EQUINOXE REVERSE 46MM GLENOSPHERE

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code KWT·October 2, 2024

    Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer Cemented

    FDA classification
    FDA Class 2 ·Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer Cemented

    UNKNOWN UNITE HUMERAL HEAD

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC. 1818910·Product code KWS·December 7, 2016

    RSP SHOULDER

    FDA Adverse Event
    Injury ·ENCORE MEDICAL, L.P.·Product code KWS·October 4, 2016

    ANATOMICAL SHOULDER REVERSE, HUMERAL INSERT, PE, 36-6

    FDA Adverse Event
    Injury ·ZIMMER GMBH·Product code KWS·October 28, 2016

    GLOBAL AP PC STEM 10 MM

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC. 1818910·Product code KWS·October 5, 2016

    PT HYBRID GLENOID POST REGENEREX POROUS TITANIUM CONSTRUCT

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWS·November 30, 2016

    AFFINITI SHOULDER SYSTEM

    FDA Adverse Event
    Injury ·TORNIER INC.·Product code KWS·December 15, 2016

    UNKNOWN COMPREHENSIVE REVERSE SHOULDER

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWS·December 1, 2016

    AEQUALIS HUMERAL HEAD

    FDA Adverse Event
    Injury ·TORNIER S.A.S.·Product code KWS·December 23, 2016

    AEQUALIS PERFORM GLENOID

    FDA Adverse Event
    Injury ·TORNIER S.A.S.·Product code KWS·October 13, 2016

    MODULAR HYBRID GLENOID BASE 4MM

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWS·December 30, 2016