BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    ADVANTAGE SERIES 29

    MDR report key: 2113655 · Received May 24, 2011

    Report

    Report Number
    1831750-2011-04982
    Event Type
    Malfunction
    Date Received
    May 24, 2011
    Date of Event
    February 1, 2010
    Report Date
    February 1, 2010
    Manufacturer
    STRYKER MEDICAL
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    MA, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Description of Event or Problem · 1

    IT WAS REPORTED BY SERVICE REPORT THAT THE WELD WAS BROKEN ON THE SIDE RAIL WHICH PREVENTED IT FROM LATCHING. IT IS UNKNOWN IF THERE WAS PATIENT INVOLVEMENT; HOWEVER, NO ADVERSE CONSEQUENCES WERE REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 ADVANTAGE SERIES 29 HOSPITAL WHEELED STRETCHER FPO STRYKER MEDICAL 1501 NA

    Patients

    Seq Age Sex Outcome Treatment
    1