BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    OB/GYN STRETCHER

    MDR report key: 2071751 · Received April 19, 2011

    Report

    Report Number
    3006697241-2011-00030
    Event Type
    Malfunction
    Date Received
    April 19, 2011
    Date of Event
    March 25, 2011
    Report Date
    March 25, 2011
    Manufacturer
    HILL-ROM DE MEXICO S DE RL DE CV
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    THE ACCOUNT REPLACED BOTH GAS SPRINGS TO REPAIR THE STRETCHER.

    Description of Event or Problem · 1

    THE ACCOUNT ALLEGED THE HEAD OF BED IS ALL THE WAY UP AND WILL NOT LOWER. NO INJURIES. HE THINKS THAT THEY HAVE THE HEAD RAISED AND THE PT IS PUSHING IN LABOR SO HARD THAT IT IS CAUSING THE GAS SPRING TO LEAK OIL AND GET LOCKED IN POSITION.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 OB/GYN STRETCHER WHEELED STRETCHER FPO HILL-ROM DE MEXICO S DE RL DE CV 8050

    Patients

    Seq Age Sex Outcome Treatment
    1 UNK