BEUDAMED
    FDA Adverse Event Death Summary report: N

    BONE CEMENT

    MDR report key: 24053592 · Received January 13, 2026

    Report

    Report Number
    MW5182110
    Event Type
    Death
    Date Received
    January 13, 2026
    Date of Event
    March 31, 2025
    Report Date
    January 6, 2026
    Manufacturer
    STRYKER INSTRUMENTS
    Product Code
    LOD
    Adverse Event
    Yes
    Report Source
    Voluntary report
    Reporter Occupation
    UNKNOWN
    Health Professional
    *

    Narratives

    Description of Event or Problem · 0

    CLINICAL ADVERSE EVENT RECEIVED FOR DEATH - PNEUMONIA. "THIS REPORT REFLECTS INFORMATION RECEIVED BY FDA IN THE FORM OF A NOTIFICATION PER 803.22 (B)(2)".

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    112804 BONE CEMENT BONE CEMENT LOD STRYKER INSTRUMENTS 61911001 RDU055

    Patients

    Seq Age Sex Outcome Treatment
    1 NA Unknown Death