BEUDAMED
    FDA Adverse Event Other Summary report: N

    BEDSIDE

    MDR report key: 2699145 · Received August 13, 2012

    Report

    Report Number
    1218087-2012-00044
    Event Type
    Other
    Date Received
    August 13, 2012
    Manufacturer
    PACE MEDICAL, INC
    Product Code
    DTE
    PMA / PMN Number
    P920032
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    UK
    Reporter Occupation
    BIOMEDICAL ENGINEER

    Narratives

    Additional Manufacturer Narrative · 1

    CUSTOMER RETURNED THE DEVICE WITH THE COMPLAINT THAT BUTTONS WERE NOT WORKING PROPERLY. THE DEVICE WAS EXAMINED AND IT WAS FOUND THAT THERE WAS A FAULTY COMPONENT. THE COMPONENT WAS REPLACED. THE DEVICE WAS RE-CALIBRATED AND FINAL TESTED. ALL TESTS WERE PASSED AND THE DEVICE WAS RETURNED TO THE CUSTOMER. REASON FOR COMPLAINT: RANDOM COMPONENT FAILURE.

    Description of Event or Problem · 1

    PACE MEDICAL WAS NOTIFIED ON 08/10/2011 BY (B)(6) VIA LETTER THAT UNIT HAD A FAULT.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 BEDSIDE TEMPORARY CARDIAC PACEMAKER DTE PACE MEDICAL, INC 4170 NA

    Patients

    Seq Age Sex Outcome Treatment
    1