BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    SECURE II MED/SURG BED

    MDR report key: 2000333 · Received February 18, 2011

    Report

    Report Number
    1831750-2011-01634
    Event Type
    Malfunction
    Date Received
    February 18, 2011
    Date of Event
    October 28, 2010
    Report Date
    October 28, 2010
    Manufacturer
    STRYKER MEDICAL
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    IL, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    RESULT - TIMING LINK, HEADBOARD, AND FOOTBOARD; SIDERAIL.

    Description of Event or Problem · 1

    IT WAS REPORTED BY SERVICE REPORT THAT THE SIDERAIL WAS DAMAGED. IT WAS FURTHER REPORTED THAT THERE WAS DAMAGE TO THE HEADBOARD AND FOOTBOARD. 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 SECURE II MED/SURG BED AC POWERED HOSPITAL BED FNL STRYKER MEDICAL 3002 NA

    Patients

    Seq Age Sex Outcome Treatment
    1