BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    MA204

    MDR report key: 2091160 · Received April 20, 2011

    Report

    Report Number
    1831750-2011-03807
    Event Type
    Malfunction
    Date Received
    April 20, 2011
    Date of Event
    September 3, 2010
    Report Date
    September 3, 2010
    Manufacturer
    STRYKER MEDICAL
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    ID, US
    Reporter Occupation
    UNKNOWN

    Narratives

    Additional Manufacturer Narrative · 1

    WELD.

    Description of Event or Problem · 1

    IT WAS REPORTED THERE WAS UNINTENDED MOVEMENT OF THE SIDERAIL.

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1 UNK