BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    TRANSTAR STRETCHER

    MDR report key: 2982215 · Received January 25, 2013

    Report

    Report Number
    1824206-2013-00688
    Event Type
    Malfunction
    Date Received
    January 25, 2013
    Date of Event
    January 14, 2013
    Report Date
    January 14, 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 TECH FOUND THE SIDE RAIL END TUBE IS BENT. THE TECH REPLACED THE SIDE RAIL END TUBE AND RATCHET RIVETS TO RESOLVE THE ISSUE.

    Description of Event or Problem · 1

    THE TECH ALLEGED THAT THE SIDE RAIL WAS NOT STAYING IN THE UPRIGHT POSITION. NO PT IMPACT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    36495 TRANSTAR STRETCHER WHEELED STRETCHER FPO HILL-ROM, INC. 8000

    Patients

    Seq Age Sex Outcome Treatment
    1