BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    GOBED II

    MDR report key: 2861171 · Received November 2, 2012

    Report

    Report Number
    1831750-2012-11436
    Event Type
    Malfunction
    Date Received
    November 2, 2012
    Date of Event
    October 6, 2012
    Report Date
    October 6, 2012
    Manufacturer
    STRYKER MEDIACL
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NY, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Description of Event or Problem · 1

    IT WAS REPORTED BY SERVICE REPORT THAT THE BED WOULD NOT ROLL DUE TO A BROKEN CASTER. NO PT INVOLVEMENT OR ADVERSE CONSEQUENCES WERE REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 GOBED II AC HOSPITAL BED FNL STRYKER MEDIACL FL28EX NA

    Patients

    Seq Age Sex Outcome Treatment
    1