BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    TRANSPORT SERIES

    MDR report key: 2932930 · Received December 28, 2012

    Report

    Report Number
    1831750-2012-13477
    Event Type
    Malfunction
    Date Received
    December 28, 2012
    Date of Event
    December 6, 2012
    Report Date
    December 6, 2012
    Manufacturer
    STRYKER MEDICAL
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    VA, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Description of Event or Problem · 1

    IT WAS REPORTED BY SERVICE REPORT THAT THE SIDE RAILS COULD NOT REMAIN LATCHED AND THE BRAKES COULD NOT REMAIN ENGAGED. NO PATIENT INVOLVEMENT OR ADVERSE CONSEQUENCES WERE REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 TRANSPORT SERIES HOSPITAL WHEELED STRETCHER FPO STRYKER MEDICAL 0721 NA

    Patients

    Seq Age Sex Outcome Treatment
    1