BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    SURGICAL TRANSTAR STRETCHER

    MDR report key: 2033243 · Received February 28, 2011

    Report

    Report Number
    1824206-2011-01160
    Event Type
    Malfunction
    Date Received
    February 28, 2011
    Date of Event
    February 4, 2011
    Report Date
    February 4, 2011
    Manufacturer
    HILL-ROM INC.
    Product Code
    FPO
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NY, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    THE TECHNICIAN REPLACED THE FOUR MISSING RATCHET RIVETS ON THE TOP RAIL TO REPAIR THE STRETCHER.

    Description of Event or Problem · 1

    INFO REC'D INDICATES THE SIDERAIL WILL NOT LATCH DUE TO FOUR MISSING RATCHET RIVETS ON THE TOP RAIL.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 SURGICAL TRANSTAR STRETCHER WHEELED STRETCHER FPO HILL-ROM INC. 8010

    Patients

    Seq Age Sex Outcome Treatment
    1