BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    EMAX 2 PLUS MOTOR

    MDR report key: 3011086 · Received March 14, 2013

    Report

    Report Number
    1045834-2013-00683
    Event Type
    Malfunction
    Date Received
    March 14, 2013
    Date of Event
    February 15, 2013
    Report Date
    February 18, 2013
    Manufacturer
    THE ANSPACH EFFORT, INC.
    Product Code
    HBC
    PMA / PMN Number
    K080802
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    MA, US
    Reporter Occupation
    NURSE

    Narratives

    Additional Manufacturer Narrative · 1

    THE DEVICE HAS NOT BEEN RECEIVED BY ANSPACH. IF ADDITIONAL INFORMATION IS RECEIVED, A SUPPLEMENTAL REPORT WILL BE SENT.

    Description of Event or Problem · 1

    REPORT RECEIVED FROM THE USA STATING THAT THE DEVICE "SHUT OFF" DURING SURGERY. THE SURGERY WAS SLIGHTLY DELAYED BUT SPECIFIC AMOUNT OF TIME WAS UNKNOWN. THE DOCTOR WAS ABLE TO CONTINUE SURGERY WITHOUT THE DEVICE DUE TO THE DOCTOR NO LONGER REQUIRING THE DRILL. THE REPORTER DECLINED PROVIDING THE PATIENT INFORMATION. THERE WERE NO INJURIES OR MEDICAL INTERVENTION REPORTED. THERE WAS NO ADDITIONAL INFORMATION PROVIDED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    108350 EMAX 2 PLUS MOTOR HBC THE ANSPACH EFFORT, INC.

    Patients

    Seq Age Sex Outcome Treatment
    1