BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    ASKU

    MDR report key: 2132037 · Received June 16, 2011

    Report

    Report Number
    2183613-2011-00242
    Event Type
    Malfunction
    Date Received
    June 16, 2011
    Manufacturer
    MEDTRONIC MILACA INC.
    Product Code
    DTE
    PMA / PMN Number
    P820003/S72
    Removal / Correction Number
    ASKU
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CO, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    THIS REPORT IS BASED SOLELY ON DEVICE RETURN AND ANALYSIS. NO INFORMATION TO SUGGEST A DEVICE-RELATED ADVERSE EVENT OR PRODUCT PROBLEM WAS RECEIVED. IF ADDITIONAL RELEVANT INFORMATION IS RECEIVED, A SUPPLEMENTAL REPORT WILL BE SUBMITTED. EVALUATION SUMMARY: (B)(4): THE DEVICE WAS RETURNED, ANALYZED AND THE ANALYSIS CONFIRMED THE CUSTOMER COMMENT REGARDING THE KEYBOARD PAD BEING OUT OF SPEC. IT WAS ALSO NOTED THAT THE UPPER AND LOWER CASES WERE BROKEN, THE BATTERY RELEASE, HEART BLOCK, HEART WIRE CONTACTS, LEAD FLEX COVER AND HEART LEAD FLEX WAS CONTAMINATED AND THE RING WAS BENT.

    Description of Event or Problem · 1

    IT WAS REPORTED THAT WHILE TESTING THE DEVICE, THERE WERE CONSISTENT "0004 ERRORS" AT POWER UP. THE DEVICE WAS RETURNED FOR SERVICING. NO PATIENT INVOLVEMENT OR COMPLICATIONS WERE REPORTED AS A RESULT OF THIS EVENT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 ASKU EXTERNAL PULSE GENERATOR DTE MEDTRONIC MILACA INC. 5388 ASKU

    Patients

    Seq Age Sex Outcome Treatment
    1 Other