BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    DURASTAR STRETCHER

    MDR report key: 2922737 · Received December 28, 2012

    Report

    Report Number
    1824206-2012-08669
    Event Type
    Malfunction
    Date Received
    December 28, 2012
    Date of Event
    December 14, 2012
    Report Date
    December 14, 2012
    Manufacturer
    HILL-ROM INC.
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NY, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Additional Manufacturer Narrative · 1

    THE TECHNICIAN ISOLATED THE ISSUE TO THE GAS SPRINGS. HE REPLACED BOTH HEAD GAS SPRINGS TO REPAIR THE BED.

    Description of Event or Problem · 1

    INFO REC'D INDICATES THE HEAD OF THE STRETCHER WILL NOT STAY IN THE LOWERED POSITION.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 DURASTAR STRETCHER WHEELED STRETCHER FPO HILL-ROM INC. 8005

    Patients

    Seq Age Sex Outcome Treatment
    1