BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    TRANSTAR STRETCHER

    MDR report key: 2221785 · Received August 17, 2011

    Report

    Report Number
    1824206-2011-04360
    Event Type
    Malfunction
    Date Received
    August 17, 2011
    Date of Event
    August 8, 2011
    Report Date
    August 15, 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

    TECH FOUND THE BENT RIGHT SIDERAIL END TUBE WAS BENT CAUSING THE SIDERAIL NOT TO STAY UP. REPLACED THE SIDERAIL TO RESOLVE THIS ISSUE. UNIT LOCATED IN REPAIR SHOP.

    Description of Event or Problem · 1

    COMPLAINT RECEIVED INDICATED THAT THE SIDERAIL WAS NOT STAYING UP. UNIT WAS IN REPAIR SHOP. 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