BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    TRANSTER STRETCHER

    MDR report key: 2760360 · Received September 20, 2012

    Report

    Report Number
    1824206-2012-05663
    Event Type
    Malfunction
    Date Received
    September 20, 2012
    Date of Event
    August 28, 2012
    Report Date
    August 28, 2012
    Manufacturer
    HILL-ROM, INC.
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CA, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    THE TECH REPLACED THE BOLT AND NUT FROM THE SIDE RAIL LATCH PLATE TO RESOLVE THE ISSUE.

    Description of Event or Problem · 1

    THE TECH ALLEGED THAT THE SIDE RAIL WOULD NOT LATCH. NO PT IMPACT.

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1