BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    16CM MIN. INVASIVE ATTACHMENT

    MDR report key: 3032916 · Received March 29, 2013

    Report

    Report Number
    1045834-2013-01044
    Event Type
    Malfunction
    Date Received
    March 29, 2013
    Date of Event
    February 9, 2011
    Report Date
    February 10, 2011
    Manufacturer
    THE ANSPACH EFFORT, INC.
    Product Code
    HBC
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CA, US
    Reporter Occupation
    NOT APPLICABLE

    Narratives

    Additional Manufacturer Narrative · 1

    THE DEVICE HAS BEEN RECEIVED BY ANSPACH. IF ADDITIONAL INFORMATION IS RECEIVED, A SUPPLEMENTAL REPORT WILL BE SENT. STN# K011444.

    Description of Event or Problem · 1

    THE REPORT RECEIVED FROM THE USA STATING THAT THE DEVICE WAS "OVERHEATING." THE DEVICE WAS NOT BEING USED IN SURGERY. THERE WAS NO REPORTED PATIENT OR USER INJURIES. THERE WAS NO ADDITIONAL INFORMATION PROVIDED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    130662 16CM MIN. INVASIVE ATTACHMENT HBC THE ANSPACH EFFORT, INC.

    Patients

    Seq Age Sex Outcome Treatment
    1