BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    ASKU

    MDR report key: 2131688 · Received June 16, 2011

    Report

    Report Number
    2183613-2011-00315
    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
    TX, US
    Reporter Occupation
    BIOMEDICAL ENGINEER

    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 ANALYSIS FOUND THAT THE UPPER CASE, LOWER CASE, BATTERY RELEASE, LEAD FLEX COVER AND BATTERY DRAWER WAS CONTAMINATED. IT WAS ALSO NOTED THAT TWO SIDE BAIL COVERS AND RING COVER WERE BROKEN, ONE SIDE BAIL WAS BENT AND THE RING WAS MISSING.

    Description of Event or Problem · 1

    IT WAS REPORTED THAT DURING ROUTINE BIOMED INSPECTION/TESTING THE TECHNICIAN FOUND CASE DAMAGE AND WOULD ALSO LIKE TO HAVE DEVICES CALIBRATED. THE DEVICE WAS RETURNED TO THE MANUFACTURER AND SUBSEQUENTLY TESTED OUT OF SPECIFICATION. NO PATIENT INVOLVEMENT WAS REPORTED WITH 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