BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    GOBED II MED/SURG BED

    MDR report key: 2890584 · Received November 21, 2012

    Report

    Report Number
    1831750-2012-12209
    Event Type
    Malfunction
    Date Received
    November 21, 2012
    Date of Event
    October 30, 2012
    Report Date
    October 30, 2012
    Manufacturer
    STRYKER MEDICAL
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NC, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Description of Event or Problem · 1

    IT WAS REPORTED BY SERVICE REPORT THAT THERE WAS FLUID INGRESS TO THE ELECTRICAL COMPONENTS. NO PT INVOLVEMENT OR ADVERSE CONSEQUENCES WERE REPORTED. SEE SCANNED PAGE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 GOBED II MED/SURG BED A/C HOSPITAL BED FNL STRYKER MEDICAL FL28C NA

    Patients

    Seq Age Sex Outcome Treatment
    1