BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    BRAVO PH CAPSULE DELIVERY DEVICE

    MDR report key: 4921010 · Received July 15, 2015

    Report

    Report Number
    9710107-2015-00190
    Event Type
    Malfunction
    Date Received
    July 15, 2015
    Date of Event
    June 25, 2015
    Report Date
    July 15, 2015
    Manufacturer
    GIVEN IMAGING LTD.
    Product Code
    FFT
    PMA / PMN Number
    K102543
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    TX, US
    Reporter Occupation
    PHYSICIAN

    Narratives

    Additional Manufacturer Narrative · 1

    THE SITE INDICATED THAT THE INCIDENT UNIT WILL BE RETURNING TO THE MANUFACTURER FOR EVALUATION WHEN ADDITIONAL INFORMATION PERTINENT TO THE INCIDENT PRESENTS ITSELF, A FOLLOW-UP REPORT WILL BE SUBMITTED. (B)(4).

    Additional Manufacturer Narrative · 1

    (B)(4).

    Description of Event or Problem · 1

    CUSTOMER REPORTED BRAVO CAPSULE FAILED TO ATTACH. THERE WAS NO HARM TO THE PATIENT OR USER.

    Description of Event or Problem · 1

    A REPEAT PROCEDURE WAS NECESSARY DUE TO THE ALLEGED DEVICE MALFUNCTION. INTERVENTION WAS NOT REQUIRED. THERE WAS NOTHING UNUSUAL ABOUT THE PATIENT OR PROCEDURE ITSELF THAT MAY HAVE LED TO THIS EVENT. AN ENDOSCOPY WAS PERFORMED PRIOR TO THE PROCEDURE AND THE ESOPHAGUS APPEARED TO BE NORMAL. THE DEVICE OPERATOR HAS BEEN PERFORMING THIS PROCEDURE FOR ONE YEAR. NO OTHER KNOWN ADVERSE EVENTS WERE REPORTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    460819 BRAVO PH CAPSULE DELIVERY DEVICE BRAVO FFT GIVEN IMAGING LTD. FGS-0313 27196Q

    Patients

    Seq Age Sex Outcome Treatment
    1