BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    MA204

    MDR report key: 1894011 · Received November 3, 2010

    Report

    Report Number
    9680128-2010-00265
    Event Type
    Malfunction
    Date Received
    November 3, 2010
    Date of Event
    October 7, 2010
    Report Date
    October 7, 2010
    Manufacturer
    STRYKER MEDICAL QUEBEC, LP
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    MN, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    IT WAS REPORTED BY SERVICE REPORT THAT THE SIDE RAIL CONTROLS FOR FOWLER UP/DOWN WORKING IN REVERSE. NO ADVERSE CONSEQUENCES HAVE BEEN REPORTED. NO INJURY REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 MA204 HOSPITAL BED, A/C POWERED, ADJUSTABLE FNL STRYKER MEDICAL QUEBEC, LP FL25E NA

    Patients

    Seq Age Sex Outcome Treatment
    1 UNK