BEUDAMED
    FDA Adverse Event Other Summary report: N

    GOBED+

    MDR report key: 1902396 · Received November 12, 2010

    Report

    Report Number
    9680128-2010-00300
    Event Type
    Other
    Date Received
    November 12, 2010
    Date of Event
    October 19, 2010
    Report Date
    October 19, 2010
    Manufacturer
    STRYKER MEDICAL QUEBEC, LP
    Product Code
    FNL
    Report Source
    Manufacturer report
    Reporter Location
    NY, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 1

    IT WAS REPORTED BY SERVICE REPORT THAT THE SIDERAIL WILL NOT RAISE UP, OTHER SIDERAILS WILL NOT LATCH PROPERLY. NO PT INVOLVEMENT OR ADVERSE CONSEQUENCES ARE REPORTED. NO INJURY REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 GOBED+ HOSPITAL BED, AC POWERED, ADJUSTABLE FNL STRYKER MEDICAL QUEBEC, LP FL20E NA

    Patients

    Seq Age Sex Outcome Treatment
    1 UNK