BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    LIT GOBED BNQ

    MDR report key: 2061875 · Received March 18, 2011

    Report

    Report Number
    1831750-2011-02602
    Event Type
    Malfunction
    Date Received
    March 18, 2011
    Date of Event
    February 21, 2011
    Report Date
    February 21, 2011
    Manufacturer
    STRYKER MEDICAL
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CA
    Reporter Occupation
    UNKNOWN

    Narratives

    Description of Event or Problem · 1

    IT WAS REPORTED THAT THE HEAD ACTUATOR WOULD NOT RISE. IT WAS REPORTED THAT THE ACTUATOR NEEDED TO BE REPLACED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 LIT GOBED BNQ A/C HOSPITAL BED FNL STRYKER MEDICAL FL23 NA

    Patients

    Seq Age Sex Outcome Treatment
    1 UNK