BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    ELECTRIC STRETCHER

    MDR report key: 1894044 · Received November 3, 2010

    Report

    Report Number
    1831750-2010-03504
    Event Type
    Malfunction
    Date Received
    November 3, 2010
    Date of Event
    October 7, 2010
    Report Date
    October 7, 2010
    Manufacturer
    STRYKER CORP., MEDICAL DIV.
    Product Code
    INK
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    VA, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Description of Event or Problem · 1

    IT WAS REPORTED BY SERVICE REPORT THAT THE HEAD JACK IS LEAKING. NO PT INVOLVEMENT OR ADVERSE CONSEQUENCES WERE REPORTED.

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1 NA