BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    PROCEDURAL STRETCHER

    MDR report key: 3130545 · Received March 14, 2013

    Report

    Report Number
    1824206-2013-01419
    Event Type
    Malfunction
    Date Received
    March 14, 2013
    Date of Event
    February 14, 2013
    Report Date
    February 14, 2013
    Manufacturer
    HILL-ROM DE MEXICO
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    Distributor report
    Reporter Location
    NE, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Description of Event or Problem · 1

    INFORMATION RECEIVED INDICATED THE FOOT HI/LO DRIFTS. REFERENCE MANUFACTURER REPORT NUMBER 3006697241-2013-00056.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    108511 PROCEDURAL STRETCHER WHEELED STRETCHER FPO HILL-ROM DE MEXICO 8000

    Patients

    Seq Age Sex Outcome Treatment
    1