BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    GOBED II MED/SURG BED

    MDR report key: 2861301 · Received November 2, 2012

    Report

    Report Number
    1831750-2012-11522
    Event Type
    Malfunction
    Date Received
    November 2, 2012
    Date of Event
    October 8, 2012
    Report Date
    October 8, 2012
    Manufacturer
    STRYKER MEDICAL
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NC, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Additional Manufacturer Narrative · 1

    RESULTS: CONTROL BOARD AND LEFT SIDERAIL HARNESS.

    Description of Event or Problem · 1

    IT WAS REPORTED BY SERVICE REPORT THAT THE BED HAD ELECTRICAL PROBLEMS DUE TO A CLEANING AGENT THAT WAS SPRAYED ON THE ELECTRICAL CONNECTORS FOR THE FOOTBOARD. NO PT INVOLVEMENT OR ADVERSE CONSEQUENCES WERE REPORTED.

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1