BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    PROCEDURAL STRETCHER

    MDR report key: 1946047 · Received December 23, 2010

    Report

    Report Number
    3006697241-2010-00060
    Event Type
    Malfunction
    Date Received
    December 23, 2010
    Date of Event
    November 24, 2010
    Report Date
    November 24, 2010
    Manufacturer
    HILL-ROM DE MEXICO S DE RL DE CV
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    IL, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    THE END TUBE WAS REPLACED TO REPAIR THE STRETCHER.

    Description of Event or Problem · 1

    THE ACCOUNT ALLEGED THE RIGHT SIDERAIL END TUBE WAS BROKEN AND THE SIDERAIL WOULD NOT LATCH AT THE UP POSITION.

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1