BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    THE FLORENCE BED

    MDR report key: 1882814 · Received October 21, 2010

    Report

    Report Number
    9680128-2010-00186
    Event Type
    Malfunction
    Date Received
    October 21, 2010
    Date of Event
    September 25, 2010
    Report Date
    September 25, 2010
    Manufacturer
    STRYKER MEDICAL QUEBEC, LP
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    ID, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    RESULT CODE DESCRIPTION: SIDERAIL MEMBRANE.

    Description of Event or Problem · 1

    IT WAS REPORTED BY SERVICE REPORT THAT THE SIDERAILS CONTROL WERE NOT RESPONDING. NO ADVERSE CONSEQUENCES HAVE BEEN REPORTED. NO INJURY REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 THE FLORENCE BED HOSPITAL BED, A-C POWERED, ADJUSTABLE FNL STRYKER MEDICAL QUEBEC, LP FL23SE NA

    Patients

    Seq Age Sex Outcome Treatment
    1 UNK