BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    SECURE ACUTE CARE BED

    MDR report key: 1964029 · Received January 12, 2011

    Report

    Report Number
    1831750-2011-00351
    Event Type
    Malfunction
    Date Received
    January 12, 2011
    Date of Event
    November 1, 2010
    Report Date
    November 1, 2010
    Manufacturer
    STRYKER CORP, MEDICAL DIV
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NV, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    IT WAS REPORTED BY SERVICE REPORT THAT THE FOOT MOTOR IS OUT AND THE FOOT END IS STUCK IN THE UP POSITION. NO PT INVOLVEMENT OR ADVERSE CONSEQUENCES ARE REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 SECURE ACUTE CARE BED AC POWERED HOSPITAL BED FNL STRYKER CORP, MEDICAL DIV 3000 NA

    Patients

    Seq Age Sex Outcome Treatment
    1