BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    GOBED II

    MDR report key: 3963715 · Received July 22, 2014

    Report

    Report Number
    1831750-2014-00001
    Event Type
    Malfunction
    Date Received
    July 22, 2014
    Date of Event
    July 31, 2012
    Report Date
    July 31, 2012
    Manufacturer
    STRYKER MEDICAL KALAMAZOO
    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 BED DRIFTS ON THE FOOT END. NO PATIENT INVOLVEMENT OR ADVERSE CONSEQUENCES ARE REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    427093 GOBED II A/C HOSPITAL BED FNL STRYKER MEDICAL KALAMAZOO FL28EX

    Patients

    Seq Age Sex Outcome Treatment
    1 UNK