BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    TRANSTAR STRETCHER

    MDR report key: 2212140 · Received July 8, 2011

    Report

    Report Number
    1824206-2011-03636
    Event Type
    Malfunction
    Date Received
    July 8, 2011
    Date of Event
    June 28, 2011
    Report Date
    June 28, 2011
    Manufacturer
    HILL-ROM, INC.
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    MS, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    TECHNICIAN FOUND THE BED IN BED SHOP WITH NOTE SAYING "BRAKES DO NOT WORK" FOUND TWO HEAD CASTERS WOULD SWIVEL WHEN THE BRAKES WERE SET. REPLACED THE TWO HEAD CASTERS TO RESOLVE THIS ISSUE.

    Description of Event or Problem · 1

    COMPLAINT REPORT RECEIVED INDICATING THAT THE BRAKES ON THE BED WERE NOT WORKING. BED IN BED SHOP. NO INJURIES ALLEGED.

    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