BEUDAMED
    FDA Adverse Event Injury Summary report: N

    HIP LINER

    MDR report key: 23619641 · Received November 21, 2025

    Report

    Report Number
    MW5179284
    Event Type
    Injury
    Date Received
    November 21, 2025
    Date of Event
    October 14, 2025
    Report Date
    October 14, 2025
    Manufacturer
    HOWMEDICA INTERNATIONAL S. DE R.L/ STRYKER CORP.
    Product Code
    LYT
    Adverse Event
    Yes
    Report Source
    Voluntary report
    Reporter Occupation
    UNKNOWN
    Health Professional
    *

    Narratives

    Description of Event or Problem · 0

    SURGEON DECIDED TO REVISE ENTIRE HIP DUE TO RECURRENT DISLOCATIONS. THIS REPORT REFLECTS INFORMATION RECEIVED BY FDA IN THE FORM OF A NOTIFICATION PER 803.22 (B)(2). PT CODE: 2374. DEVICE CODE: 4002. REF REPORT: MW5179283.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    2629183 HIP LINER FIXATION ACCESSORY LYT HOWMEDICA INTERNATIONAL S. DE R.L/ STRYKER CORP.

    Patients

    Seq Age Sex Outcome Treatment
    1 NA Unknown