BEUDAMED
    FDA Adverse Event Injury Summary report: N

    DEPUY INHANCE REVERSE SHOULDER SYSTEM

    MDR report key: 22730878 · Received August 6, 2025

    Report

    Report Number
    MW5174144
    Event Type
    Injury
    Date Received
    August 6, 2025
    Date of Event
    July 29, 2025
    Report Date
    July 30, 2025
    Manufacturer
    DEPUY IRELAND UC
    Product Code
    PHX
    Adverse Event
    Yes
    Report Source
    Voluntary report
    Reporter Location
    MO, US
    Reporter Occupation
    003
    Health Professional
    N

    Narratives

    Description of Event or Problem · 0

    INVESTIGATIONAL DEVICE, DEPUY INHANCE REVERSE STEMLESS SHOULDER IMPLANT, HAD TO BE REVISED DUE TO PERIPROSTHETIC FRACTURE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    505558 DEPUY INHANCE REVERSE SHOULDER SYSTEM SHOULDER PROSTHESIS, REVERSE CONFIGURATION PHX DEPUY IRELAND UC 5200-00-036 652705

    Patients

    Seq Age Sex Outcome Treatment
    1 NA Female Hospitalization| R