BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    *

    MDR report key: 3231185 · Received May 28, 2013

    Report

    Report Number
    3231185
    Event Type
    Malfunction
    Date Received
    May 28, 2013
    Date of Event
    May 18, 2013
    Report Date
    May 28, 2013
    Manufacturer
    STRYKER MEDICAL
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    User Facility report
    Reporter Location
    RI, US
    Reporter Occupation
    INVALID DATA

    Narratives

    Description of Event or Problem · 1

    HEAD OF BED DOES NOT RISE ABOVE 20% ANGLE.WHAT WAS THE ORIGINAL INTENDED PROCEDURE?NA.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    233521 * BED FNL STRYKER MEDICAL * *

    Patients

    Seq Age Sex Outcome Treatment
    1 90 YR