BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    GOBED II

    MDR report key: 2913974 · Received January 14, 2013

    Report

    Report Number
    0001831750-2013-00063
    Event Type
    Malfunction
    Date Received
    January 14, 2013
    Date of Event
    December 28, 2012
    Report Date
    December 28, 2012
    Manufacturer
    STRYKER
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NY, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    IT WAS REPORTED BY SERVICE REPORT THAT THE POWER CORD WAS DAMAGED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    20367 GOBED II BED, AC-POWERED ADJUSTABLE HOSPITAL FNL STRYKER

    Patients

    Seq Age Sex Outcome Treatment
    1