BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    ELECTRIC STRETCHER

    MDR report key: 2110305 · Received May 20, 2011

    Report

    Report Number
    1831750-2011-04930
    Event Type
    Malfunction
    Date Received
    May 20, 2011
    Date of Event
    April 23, 2011
    Report Date
    April 23, 2011
    Manufacturer
    STRYKER MEDICAL
    Product Code
    INK
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NY, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    IT WAS REPORTED BY SERVICE REPORT THAT THE STRETCHER'S SIDE RAILS HAVE BROKEN TOP RAILS PRESENTING SHARP EDGES. NO PT INVOLVEMENT OR ADVERSE CONSEQUENCES ARE REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 ELECTRIC STRETCHER HOSPITAL WHEELED STRETCHER INK STRYKER MEDICAL 1550 NA

    Patients

    Seq Age Sex Outcome Treatment
    1