BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    POWER DRIVE

    MDR report key: 4101700 · Received September 19, 2014

    Report

    Report Number
    8030965-2014-01426
    Event Type
    Malfunction
    Date Received
    September 19, 2014
    Report Date
    December 4, 2012
    Manufacturer
    SYNTHES GMBH
    Product Code
    GEY
    PMA / PMN Number
    EXEMPT
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NL
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    SYNTHES IS SUBMITTING THIS REPORT AS A RESULT OF REMEDIATION ACTIVITIES RELATED TO SYNTHES OUS SERVICE AND REPAIR FILES LEGACY REVIEW/REMEDIATION PROTOCOL-COMPLAINT HANDLING AND MDR REPORTING. DEVICE LISTED IN THIS REPORT IS USED FOR TREATMENT, NOT DIAGNOSIS. ANY ADDITIONAL INFORMATION RECEIVED REGARDING THIS EVENT AFTER FILING THIS REPORT SHALL BE FILED ON A SUPPLEMENTAL MDR. (B)(6). DURING PRE-REPAIR ASSESSMENT PERFORMED BY TECHNICIAN, FUNCTIONAL TESTING WAS PERFORMED AND REVEALED THE CONTROL UNIT WAS NOT FUNCTIONING. MAINTENANCE WAS PERFORMED AND PARTS WERE REPLACED. DEVICE WAS RETURNED TO THE CUSTOMER ON (B)(6) 2012. PLACEHOLDER.

    Description of Event or Problem · 1

    CUSTOMER REPORTED POWER DRIVE GETS HOT WITHOUT USING. THIS IS REPORT 1 OF 1 FOR COMPLAINT (B)(4).

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    584784 POWER DRIVE GEY SYNTHES GMBH 36425

    Patients

    Seq Age Sex Outcome Treatment
    1