BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    BRAVO

    MDR report key: 1021623 · Received March 26, 2008

    Report

    Report Number
    2032545-2008-01592
    Event Type
    Malfunction
    Date Received
    March 26, 2008
    Date of Event
    February 25, 2008
    Report Date
    February 25, 2008
    Manufacturer
    ARIZONA DEVICE MANUFACTURING
    Product Code
    FFT
    PMA / PMN Number
    K002028
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NJ, US
    Reporter Occupation
    NURSE

    Narratives

    Additional Manufacturer Narrative · 1

    THE DEVICE IS INCLUDED IN THE BRAVO PH CAPSULE AND DELIVERY SYSTEM 9012B1011. (5-PACK) AND 9012B1001 (SINGLE PACK) FIELD ACTION- FAILURE TO DETACH, PHYSICIAN COMMUNICATION (03-DECEMBER-2007).

    Description of Event or Problem · 1

    IT WAS REPORTED THAT WHILE PACING THE BRAVO PH MONITOR, THE CAPSULE WOULD NOT DEPLOY FROM THE DELIVERY SYSTEM. NO SERIOUS INJURY TO THE PT WAS REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 BRAVO FFT ARIZONA DEVICE MANUFACTURING 9012B1001 Q207310

    Patients

    Seq Age Sex Outcome Treatment
    1 UNK