BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    CARELINK

    MDR report key: 3153538 · Received June 8, 2013

    Report

    Report Number
    2182208-2013-01447
    Event Type
    Malfunction
    Date Received
    June 8, 2013
    Date of Event
    March 26, 2013
    Report Date
    March 26, 2013
    Manufacturer
    MEDTRONIC, INC.
    Product Code
    DXY
    PMA / PMN Number
    P890003
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    MN, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    PRODUCT EVENT SUMMARY: ANALYSIS CONFIRMED THE KEYBOARD LID WAS LOOSE AND NEEDED REPAIR. THE PROGRAMMER DID NOT COMMUNICATE WITH THE ANALYZER. THE PROGRAMMER DOES COMMUNICATE WITH A KNOWN GOOD ANALYZER. IT WAS ALSO NOTED THAT THE TABS ON THE POWER CORD DOOR WERE BROKEN OFF.

    Additional Manufacturer Narrative · 1

    THE INFORMATION SUBMITTED REFLECTS ALL RELEVANT DATA RECEIVED. IF ADDITIONAL RELEVANT INFORMATION IS RECEIVED, A SUPPLEMENTAL REPORT WILL BE SUBMITTED. CONCOMITANT PRODUCTS: PRODUCT ID 2067L RF HEAD; PRODUCT ID R2290 ANALYZER. (B)(4).

    Additional Manufacturer Narrative · 1

    IF INFORMATION IS PROVIDED IN THE FUTURE, A SUPPLEMENTAL REPORT WILL BE ISSUED.

    Description of Event or Problem · 1

    IT WAS REPORTED THE SCREW COULD NOT BE RETRACTED TO CHECK THE ANALYZER. THE ANALYZER IS NOT CONNECTED. THE ANALYZER WAS TURNED ON TO DO A CASE/CHECK/TEST AND UNABLE TO FIX. IT WAS ALSO REPORTED THE LID TO KEYBOARD NEEDS TO BE REPAIR. THE ANALYZER AND PROGRAMMER WERE RETURNED FOR REPAIR. NO PATIENT COMPLICATIONS WERE REPORTED AS A RESULT OF THIS EVENT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    256885 CARELINK PULSE-GENERATOR, PACEMAKER, IMPLANTABLE DXY MEDTRONIC, INC. 2090W

    Patients

    Seq Age Sex Outcome Treatment
    1