BEUDAMED
    FDA Adverse Event Death Summary report: N

    DE PUY

    MDR report key: 624775 · Received May 31, 2005

    Report

    Report Number
    MW1035632
    Event Type
    Death
    Date Received
    May 31, 2005
    Date of Event
    May 26, 2005
    Report Date
    May 31, 2005
    Manufacturer
    *
    Product Code
    LXH
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    OH, US
    Reporter Occupation
    OTHER HEALTH CARE PROFESSIONAL

    Narratives

    Description of Event or Problem · 1

    REQUESTED STERILIZATION INSTRUCTIONS FROM DE PUY FOR THE ORTHOPEDIC LOANER SETS. THE MFR CLAIMS THEY DO NOT HAVE STERILIZATION INSTRUCTIONS.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 DE PUY ORTHOPEDIC LOANER SETS LXH * LOANER SETS *

    Patients

    Seq Age Sex Outcome Treatment
    1 * Death| H| L| S