BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    SECURE 3 MED/SURG BED

    MDR report key: 1830061 · Received September 7, 2010

    Report

    Report Number
    1831750-2010-02119
    Event Type
    Malfunction
    Date Received
    September 7, 2010
    Date of Event
    July 15, 2010
    Report Date
    August 13, 2010
    Manufacturer
    STRYKER CORP., MEDICAL DIV.
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CI
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    IT WAS REPORTED THAT THE CPU BOARD MALFUNCTIONED AFFECTING EITHER THE FOOT END OR THE HEAD END. IT COULD NOT BE CONFIRMED WHICH END WAS AFFECTED OR WHICH POSITION IT WAS STUCK IN. NO ADVERSE CONSEQUENCES REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 SECURE 3 MED/SURG BED A/C POWERED HOSPITAL BED FNL STRYKER CORP., MEDICAL DIV. 3002S3 NA

    Patients

    Seq Age Sex Outcome Treatment
    1