BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    TRANSTAR STRETCHER

    MDR report key: 3061555 · Received March 27, 2013

    Report

    Report Number
    1824206-2013-01727
    Event Type
    Malfunction
    Date Received
    March 27, 2013
    Date of Event
    February 27, 2013
    Report Date
    February 27, 2013
    Manufacturer
    HILL-ROM, INC.
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NY, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Additional Manufacturer Narrative · 1

    THE HILL-ROM TECHNICIAN INDICATED THE CASTERS WERE WORN OUT. HE REPLACED THE CASTERS TO RESOLVE THE ISSUE.

    Description of Event or Problem · 1

    INFO RECEIVED INDICATED THE CASTERS WOULD SWIVEL IN BRAKE MODE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    125255 TRANSTAR STRETCHER WHEELED STRETCHER FPO HILL-ROM, INC. 8005

    Patients

    Seq Age Sex Outcome Treatment
    1