BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    MICROMAX-PLUS MOTOR ASSY

    MDR report key: 4182561 · Received October 17, 2014

    Report

    Report Number
    1045834-2014-14133
    Event Type
    Malfunction
    Date Received
    October 17, 2014
    Report Date
    July 24, 2012
    Manufacturer
    DEPUY SYNTHES POWER TOOLS
    Product Code
    ERL
    PMA / PMN Number
    PK965080
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    SZ
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    ADDITIONAL NARRATIVE: 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. DURING PRE-REPAIR ASSESSMENT PERFORMED BY A TECHNICIAN, THE DEVICE WAS FOUND TO BE NOT FUNCTIONING PROPERLY AND SOME PARTS REQUIRED REPLACING; THE CAUSE IS UNDETERMINED. DEVICE WAS REPAIRED AND RETURNED TO THE CUSTOMER.

    Description of Event or Problem · 1

    IT WAS REPORTED THAT THE ATTACHMENT IS HARD TO CONNECT AND THAT THE DEVICE OVERHEATED. THIS IS REPORT 1 OF 1 FOR (B)(4).

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    660224 MICROMAX-PLUS MOTOR ASSY DRILL, SURGICAL, ENT (PNEUMATIC) - HANDPIECE ERL DEPUY SYNTHES POWER TOOLS 050000224894

    Patients

    Seq Age Sex Outcome Treatment
    1