BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    SECURE II MED/SURG BED

    MDR report key: 1840391 · Received September 10, 2010

    Report

    Report Number
    1831750-2010-02322
    Event Type
    Malfunction
    Date Received
    September 10, 2010
    Date of Event
    August 18, 2010
    Report Date
    August 18, 2010
    Manufacturer
    STRYKER CORP, MEDICAL DIV.
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    FL, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    IT WAS REPORTED IN SERVICE REPORT THAT THERE WAS MISSING COMMUNICATION CORD AND THE BED EXIT ALARM WAS NOT WORKING. NO ADVERSE CONSEQUENCES WERE 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 NA

    Patients

    Seq Age Sex Outcome Treatment
    1