BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    S3 EX - 3005

    MDR report key: 2904483 · Received November 30, 2012

    Report

    Report Number
    1831750-2012-12245
    Event Type
    Malfunction
    Date Received
    November 30, 2012
    Date of Event
    November 5, 2012
    Report Date
    November 5, 2012
    Manufacturer
    STRYKER MEDICAL
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CA, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Additional Manufacturer Narrative · 1

    RESULTS: IBED AWARENESS NOT CONFIGURED TO BE ON.

    Description of Event or Problem · 1

    IT WAS REPORTED BY SERVICE REPORT THAT IBED AWARENESS WAS NOT FUNCTIONING. NO PATIENT INVOLVEMENT OR ADVERSE CONSEQUENCES WERE REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 S3 EX - 3005 A/C POWERED HOSPITAL BED FNL STRYKER MEDICAL 3005 NA

    Patients

    Seq Age Sex Outcome Treatment
    1