BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    PROCEDURAL STRETCHER

    MDR report key: 3130564 · Received March 27, 2013

    Report

    Report Number
    1824206-2013-01728
    Event Type
    Malfunction
    Date Received
    March 27, 2013
    Date of Event
    February 27, 2013
    Report Date
    February 27, 2013
    Manufacturer
    HILL-ROM DE MEXICO S DE RL DE CV
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    Distributor report
    Reporter Location
    OH, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    THE TECHNICIAN ALLEGED THAT THE SCALE HEAD HAS FLUID IN IT. NO INJURY REPORTED. REFERENCE MFR REPORT # 3006697241-2013-00067.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    127348 PROCEDURAL STRETCHER WHEELED STRETCHER FPO HILL-ROM DE MEXICO S DE RL DE CV 8000

    Patients

    Seq Age Sex Outcome Treatment
    1