BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    TRANSTAR STRETCHER

    MDR report key: 3130524 · Received February 25, 2013

    Report

    Report Number
    1824206-2013-01097
    Event Type
    Malfunction
    Date Received
    February 25, 2013
    Date of Event
    January 29, 2013
    Report Date
    January 29, 2013
    Manufacturer
    HILL-ROM DE MEXICO S DE RL DE CV
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    Distributor report
    Reporter Location
    TX, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    THE TECHNICIAN ALLEGED THAT THE HEAD SECTION DOES NOT LOWER COMPLETELY DOWN. NO INJURY REPORTED. REFERENCE MANUFACTURER REPORT NUMBER 3006697241-2013-00040.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    81157 TRANSTAR STRETCHER WHEELED STRETCHER FPO HILL-ROM DE MEXICO S DE RL DE CV 8000

    Patients

    Seq Age Sex Outcome Treatment
    1