BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    ADULT ROTATING CRANIOTOME

    MDR report key: 3984254 · Received December 18, 2013

    Report

    Report Number
    1045834-2013-16162
    Event Type
    Malfunction
    Date Received
    December 18, 2013
    Date of Event
    April 14, 2011
    Report Date
    May 6, 2011
    Manufacturer
    DEPUY SYNTHES POWER TOOLS
    Product Code
    HBC
    PMA / PMN Number
    K011444
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    PL
    Reporter Occupation
    NOT APPLICABLE

    Narratives

    Additional Manufacturer Narrative · 1

    THE DEVICE HAS BEEN RECEIVED BY DEPUY SYNTHES POWER TOOLS. THE INVESTIGATION IS STILL IN PROCESS. WHEN THE INVESTIGATION HAS BEEN COMPLETED OR ADDITIONAL INFO BECOMES AVAILABLE, A SUPPLEMENTAL REPORT WILL BE SENT.

    Description of Event or Problem · 1

    REPORT RECEIVED FROM (B)(6) STATING THAT NOISE WAS COMING FROM THE DEVICE. THE DEVICE WAS BEING USED DURING SURGERY. NO USER OR PT INJURY OCCURRED. IT IS UNK IF MEDICAL INTERVENTION OCCURRED. THERE WAS NO ADDITIONAL INFO PROVIDED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    663831 ADULT ROTATING CRANIOTOME HBC DEPUY SYNTHES POWER TOOLS

    Patients

    Seq Age Sex Outcome Treatment
    1