BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    ELECTRIC STRETCHER 12/09

    MDR report key: 1982341 · Received January 13, 2011

    Report

    Report Number
    1831750-2011-00482
    Event Type
    Malfunction
    Date Received
    January 13, 2011
    Date of Event
    December 9, 2010
    Report Date
    December 9, 2010
    Manufacturer
    STRYKER CORP, MEDICAL DIV.
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NY, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Description of Event or Problem · 1

    IT WAS REPORTED BY SERVICE REPORT THAT THE POWER CORD WIRES INSIDE WERE EXPOSED. IT IS UNK IF THERE WAS PT INVOLVEMENT OR IF THERE ARE ADVERSE CONSEQUENCES TO REPORT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 ELECTRIC STRETCHER 12/09 HOSPITAL WHEELED STRETCHER FNL STRYKER CORP, MEDICAL DIV. 1550 NA

    Patients

    Seq Age Sex Outcome Treatment
    1 UNK