BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    GOBED+

    MDR report key: 2800248 · Received October 8, 2012

    Report

    Report Number
    1831750-2012-10533
    Event Type
    Malfunction
    Date Received
    October 8, 2012
    Date of Event
    September 11, 2012
    Report Date
    September 11, 2012
    Manufacturer
    STRYKER MEDICAL
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CO, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Additional Manufacturer Narrative · 1

    RESULTS: SIDERAIL WELD DAMAGED.

    Description of Event or Problem · 1

    IT WAS REPORTED BY SERVICE REPORT THAT THE SIDE RAIL HAS A BROKEN WELD. NO PATIENT 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