BEUDAMED
    FDA Adverse Event Other Summary report: N

    XENFORM

    MDR report key: 3935875 · Received June 26, 2014

    Report

    Report Number
    3004170064-2014-00137
    Event Type
    Other
    Date Received
    June 26, 2014
    Report Date
    June 26, 2014
    Manufacturer
    TEI BIOSCIENCES INC.
    Product Code
    FTM
    PMA / PMN Number
    060984
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Occupation
    NOT APPLICABLE

    Narratives

    Description of Event or Problem · 1

    THIS IS BEING REPORTED AS AN ADVERSE EVEN BECAUSE THE COMPLAINT ORIGINATED FROM AN ATTORNEY. IT IS NOT KNOWN WHAT THE PATIENT WAS ORIGINALLY TREATED FOR. TWO DEVICES WERE IMPLANTED ON (B)(6) 2014. NO ADDITIONAL INFORMATION WAS PROVIDED. THE COMPLAINT VIA THE ATTORNEY WAS THAT THE PATIENT SUFFERED AN INJURY (UNSPECIFIED). IT IS NOT KNOWN WHEN THE EVENT OCCURRED. IT IS NOT KNOWN WHAT THE PATIENT'S CURRENT IS. NO INFORMATION HAS BEEN CONFIRMED BY A HEALTH CARE PROFESSIONAL. (BECAUSE TWO DEVICES WERE IMPLANTED A SECOND REPORT HAS BEEN GENERATED - 3004170064-2014-00136).

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    375195 XENFORM SURGICAL MESH FTM TEI BIOSCIENCES INC.

    Patients

    Seq Age Sex Outcome Treatment
    1 UNK Other