BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    SECURE II MED/SURG BED

    MDR report key: 1874950 · Received October 13, 2010

    Report

    Report Number
    1831750-2010-02826
    Event Type
    Malfunction
    Date Received
    October 13, 2010
    Date of Event
    September 16, 2010
    Report Date
    September 16, 2010
    Manufacturer
    STRYKER CORP. MEDICAL DIV.
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CA, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    AN INCOMPATIBLE FOOTBOARD HAD BEEN PLACED ON THE UNIT WHICH AFFECTED THE FOOTBOARD'S FUNCTIONALITY.

    Description of Event or Problem · 1

    IT WAS REPORTED BY SERVICE REPORT THAT THE BED HAD THE WRONG FOOTBOARD. NO ADVERSE CONSEQUENCES HAVE BEEN REPORTED.

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1