BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    TRANSTAR STRETCHER

    MDR report key: 2253781 · Received August 10, 2011

    Report

    Report Number
    1824206-2011-04225
    Event Type
    Malfunction
    Date Received
    August 10, 2011
    Date of Event
    July 28, 2011
    Report Date
    August 1, 2011
    Manufacturer
    HILL-ROM INC.
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NY, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    TECHNICIAN FOUND THAT THE LEFT SIDERAIL WOULD NOT STAY UP, OR LATCH CORRECTLY. REPLACED END TUBE TO RESOLVE THIS ISSUE.

    Description of Event or Problem · 1

    COMPLAINT THAT THE LEFT SIDERAIL DOES NOT STAY UP. NO INJURY REPORTED.

    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