BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    BRAVO

    MDR report key: 2011948 · Received February 10, 2011

    Report

    Report Number
    9710107-2011-00067
    Event Type
    Malfunction
    Date Received
    February 10, 2011
    Date of Event
    January 11, 2011
    Report Date
    February 10, 2011
    Manufacturer
    GIVEN IMAGING LTD.
    Product Code
    FFT
    PMA / PMN Number
    K002028
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    IS
    Reporter Occupation
    NOT APPLICABLE

    Narratives

    Description of Event or Problem · 1

    CUSTOMER REPORTED ON A BRAVO PH CAPSULE THAT FAILED TO ATTACH. ACCORDING TO CUSTOMER, WHEN THE PHYSICIAN WAS ATTEMPTING TO PLACE THE CAPSULE, THE HANDLE BROKE DURING PLACING. THE PLUNGER AND SPRING POPPED OUT WHEN ACTIVATED. THE PATIENT WAS NOT INJURED FOLLOWING THE PROCEDURE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 BRAVO BRAVO PH CAPSULE FFT GIVEN IMAGING LTD. BRAVO PH CAPSULE 14101Q

    Patients

    Seq Age Sex Outcome Treatment
    1 Required Intervention