BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    HISTOACRYL BLUE 0.5ML

    MDR report key: 8528939 · Received April 18, 2019

    Report

    Report Number
    3003639970-2019-00371
    Event Type
    Malfunction
    Date Received
    April 18, 2019
    Report Date
    April 18, 2019
    Manufacturer
    B.BRAUN SURGICAL SA
    Product Code
    MPN
    PMA / PMN Number
    SEE H10
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    CH
    Reporter Occupation
    OTHER HEALTH CARE PROFESSIONAL

    Narratives

    Additional Manufacturer Narrative · 0

    AESCULAP INC. (IMPORTER) IS SUBMITTING THIS REPORT ON BEHALF OF B. BRAUN SURGICAL S.A. (MANUFACTURER). EXEMPTION NUMBER: E2014012 REPORTED DEVICE NOT MARKETED IN THE U.S., HOWEVER, SIMILAR DEVICES OR DEVICES THAT SHARE COMPONENTS, RAW MATERIALS, PROCESS METHODS OR OTHER TECHNOLOGICAL CHARACTERISTICS ARE REGISTERED WITHIN THE U.S. K11959 IF ADDITIONAL INFORMATION IS RECEIVED A FOLLOW UP REPORT WILL BE SUBMITTED.

    Description of Event or Problem · 0

    IT WAS REPORTED LEAKAGE OCCURRED. THE REPORTER INDICATED THAT WHEN OPENING THE PACKAGE, IT WAS FOUND THAT TWO AMPULES HAD LEAKAGE. NO OTHER INFORMATION HAS BEEN PROVIDED. ASSOCIATED MEDWATCHES: 3003639970-2019-00356, 3003639970-2019-00371 (SECOND AMPULE).

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    321849 HISTOACRYL BLUE 0.5ML TISSUE ADHESIVES MPN B.BRAUN SURGICAL SA 1050044 217393N2

    Patients

    Seq Age Sex Outcome Treatment
    1