BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    LTC MED SURG BED

    MDR report key: 3821496 · Received May 20, 2014

    Report

    Report Number
    0001831750-2014-02999
    Event Type
    Malfunction
    Date Received
    May 20, 2014
    Date of Event
    April 28, 2014
    Report Date
    April 28, 2014
    Manufacturer
    STRYKER MEDICAL-KALAMAZOO
    Product Code
    FNL
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CA
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    CONCLUSION - CUSTOMER SENT PARTS TO PERFORM REPAIRS. INSPECTED BY CUSTOMER.

    Description of Event or Problem · 1

    IT WAS REPORTED THAT THE LIFT WAS STUCK ELEVATED DUE TO A FAULTY MOTOR. NO PATIENT WAS AFFECTED AND NO ADVERSE CONSEQUENCE OR CLINICALLY RELEVANT DELAY IN TREATMENT WAS REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    300471 LTC MED SURG BED BED, AC-POWERED ADJUSTABLE HOSPITAL FNL STRYKER MEDICAL-KALAMAZOO

    Patients

    Seq Age Sex Outcome Treatment
    1