BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    TRANSTAR STRETCHER

    MDR report key: 1852005 · Received September 24, 2010

    Report

    Report Number
    1824206-2010-10120
    Event Type
    Malfunction
    Date Received
    September 24, 2010
    Date of Event
    August 31, 2010
    Report Date
    August 31, 2010
    Manufacturer
    HILL-ROM INC.
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    TX, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Additional Manufacturer Narrative · 1

    TECHNICIAN INSPECTED THE PATIENT LEFT SIDERAIL AND FOUND THAT THE SCREW AND BOLT THAT SECURE THE SIDERAIL TO THE SIDERAIL LATCH WERE MISSING. TECHNICIAN REPLACED THE SCREW AND BOLT THUS SECURING THE SIDERAIL AND SIDERAIL LATCH TOGETHER. THE SIDERAIL NOW OPERATES PROPERLY.

    Description of Event or Problem · 1

    ACCOUNT ALLEGED THAT THE STRETCHER HAD A BROKEN SIDERAIL. THERE WAS NO PATIENT IMPACT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 TRANSTAR STRETCHER WHEELED STRETCHER FPO HILL-ROM INC. P8000

    Patients

    Seq Age Sex Outcome Treatment
    1