BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    GOBED II

    MDR report key: 1894033 · Received November 3, 2010

    Report

    Report Number
    9680128-2010-00262
    Event Type
    Malfunction
    Date Received
    November 3, 2010
    Date of Event
    September 29, 2010
    Report Date
    September 29, 2010
    Manufacturer
    STRYKER MEDICAL QUEBEC, LP
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    WA, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    IT WAS REPORTED THAT THE WALL SAVER IS NOT WORKING. NO ADVERSE CONSEQUENCES WERE REPORTED. NO INJURY REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 GOBED II HOSPITAL BED, A-C POWERED, ADJUSTABLE FNL STRYKER MEDICAL QUEBEC, LP FL28EX NA

    Patients

    Seq Age Sex Outcome Treatment
    1 UNK