BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    OEM STRETCHER CONFIGS

    MDR report key: 2113661 · Received May 24, 2011

    Report

    Report Number
    1831750-2011-04979
    Event Type
    Malfunction
    Date Received
    May 24, 2011
    Date of Event
    April 25, 2011
    Report Date
    April 25, 2011
    Manufacturer
    STRYKER MEDICAL
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    FL, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Description of Event or Problem · 1

    IT WAS REPORTED BY SERVICE REPORT THAT THE FOOT END IS DRIFTING. NO PATIENT INVOLVEMENT OR ADVERSE CONSEQUENCES ARE REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 OEM STRETCHER CONFIGS HOSPITAL WHEELED STRETCHER FPO STRYKER MEDICAL 0722 NA

    Patients

    Seq Age Sex Outcome Treatment
    1