BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    TRANSTAR STRETCHER

    MDR report key: 2760329 · Received September 20, 2012

    Report

    Report Number
    1824206-2012-05666
    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
    VA, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    THE TECH REPLACED THE SIDE RAIL SHOULDER BOLT TO RESOLVE THE ISSUE.

    Description of Event or Problem · 1

    TECH ALLEGED THAT THE SIDE RAIL SHOULDER BOLT FOR THE LATCH WAS MISSING AND THE SIDE RAIL WOULD NOT LATCH. NO PT IMPACT.

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1