BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    UNIV-BATTERY CHARGER F/SYNTHES BATT 4 CH

    MDR report key: 4143490 · Received October 6, 2014

    Report

    Report Number
    8030965-2014-00630
    Event Type
    Malfunction
    Date Received
    October 6, 2014
    Report Date
    May 29, 2013
    Manufacturer
    SYNTHES GMBH
    Product Code
    MOQ
    PMA / PMN Number
    EXEMPT
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    GM
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    SYNTHES IS SUBMITTING THIS REPORT AS A RESULT OF REMEDIATION ACTIVITIES RELATED TO (B)(4) AND REPAIR FILES LEGACY REVIEW/REMEDIATION PROTOCOL-COMPLAINT HANDLING AND MDR REPORTING. BLANK FIELDS ON THIS FORM INDICATE THE INFORMATION IS UNKNOWN, UNAVAILABLE OR UNCHANGED. 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. DURING PRE-REPAIR ASSESSMENT PERFORMED BY TECHNICIAN, FUNCTIONAL TESTING WAS PERFORMED AND REVEALED THE HOUSING WAS BROKEN. THIS WAS CONTRIBUTED TO FAULTY HANDLING OF THE DEVICE. MAINTENANCE WAS PERFORMED. DEVICE WAS REPAIRED AND RETURNED TO THE CUSTOMER ON 06/16/2013. PLACEHOLDER.

    Description of Event or Problem · 1

    CUSTOMER REPORTED THAT THE RIGHT DUAL DEPARTMENT WAS NOT WORKING. THIS IS REPORT 1 OF 1 FOR COMPLAINT #(B)(4).

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    623211 UNIV-BATTERY CHARGER F/SYNTHES BATT 4 CH MOQ SYNTHES GMBH 44700

    Patients

    Seq Age Sex Outcome Treatment
    1