BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    REJUVENATE

    MDR report key: 3111634 · Received May 7, 2013

    Report

    Report Number
    MW5030125
    Event Type
    Malfunction
    Date Received
    May 7, 2013
    Report Date
    May 7, 2013
    Manufacturer
    STRYKER
    Product Code
    JDI
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Location
    OR, US
    Reporter Occupation
    RISK MANAGER

    Narratives

    Description of Event or Problem · 1

    PRODUCT RECALL - STRYKER REJUVENATE HIP PROSTHESIS.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    199816 REJUVENATE HIP PROSTHESIS JDI STRYKER

    Patients

    Seq Age Sex Outcome Treatment
    1 57 YR