BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    MA204

    MDR report key: 1932725 · Received November 30, 2010

    Report

    Report Number
    9680128-2010-00353
    Event Type
    Malfunction
    Date Received
    November 30, 2010
    Date of Event
    November 5, 2010
    Report Date
    November 5, 2010
    Manufacturer
    STRYKER MEDICAL QUEBEC LP
    Product Code
    FNL
    Product Problem
    Yes
    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 HEAD OF BED WILL NOT GO DOWN FULLY. NO PT INVOLVEMENT OR ADVERSE CONSEQUENCES ARE 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