BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    GOBED+

    MDR report key: 2110298 · Received May 20, 2011

    Report

    Report Number
    1831750-2011-04894
    Event Type
    Malfunction
    Date Received
    May 20, 2011
    Date of Event
    April 25, 2011
    Report Date
    April 25, 2011
    Manufacturer
    STRYKER MEDICAL
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    IA, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Description of Event or Problem · 1

    IT WAS REPORTED BY SERVICE REPORT THAT THE HEAD LEFT, AND FOOT LEFT SIDERAILS ARE BROKEN. NO PT INVOLVEMENT OR ADVERSE CONSEQUENCES ARE REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 GOBED+ A/C HOSPITAL BED FNL STRYKER MEDICAL FL20E NA

    Patients

    Seq Age Sex Outcome Treatment
    1 UNK