BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    TRANSPORT SERIES OBS10/25/04

    MDR report key: 2913874 · Received January 14, 2013

    Report

    Report Number
    0001831750-2013-00053
    Event Type
    Malfunction
    Date Received
    January 14, 2013
    Date of Event
    December 20, 2012
    Report Date
    December 20, 2012
    Manufacturer
    STRYKER MEDICAL-KALAMAZOO
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    OK, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    IT WAS REPORTED BY SERVICE REPORT THAT THE FOOT END BRAKES WERE NOT HOLDING.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    19850 TRANSPORT SERIES OBS10/25/04 WHEELED, STRETCHER FPO STRYKER MEDICAL-KALAMAZOO 0721

    Patients

    Seq Age Sex Outcome Treatment
    1