BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    TRANSTAR STRETCHER

    MDR report key: 3162410 · Received May 30, 2013

    Report

    Report Number
    1824206-2013-02907
    Event Type
    Malfunction
    Date Received
    May 30, 2013
    Date of Event
    March 8, 2013
    Report Date
    May 20, 2013
    Manufacturer
    HILL-ROM DE MEXICO S DE RL DE CV
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    Distributor report
    Reporter Location
    FR
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    THE ACCOUNT ALLEGED THE BRAKES WOULD NOT HOLD ON ONE SIDE ONLY. NO INJURY REPORTED. PLEASE REFER MFR REPORT # 3006697241-2013-00120.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    238308 TRANSTAR STRETCHER WHEELED STRETCHER FPO HILL-ROM DE MEXICO S DE RL DE CV UNK *

    Patients

    Seq Age Sex Outcome Treatment
    1 *