BEUDAMED
    FDA Adverse Event Injury Summary report: N

    UNK URETEX MESH PRODUCT

    MDR report key: 3569425 · Received January 2, 2014

    Report

    Report Number
    9615742-2013-02530
    Event Type
    Injury
    Date Received
    January 2, 2014
    Date of Event
    July 2, 2003
    Report Date
    December 23, 2013
    Manufacturer
    SOFRADIM PRODUCTION
    Product Code
    OTN
    Adverse Event
    Yes
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    MO, US
    Reporter Occupation
    OTHER

    Narratives

    Additional Manufacturer Narrative · 1

    (B)(4). COVIDIEN IS SUBMITTING THIS REPORT ON BEHALF OF (B)(4), (IMPORTER). (B)(4).

    Additional Manufacturer Narrative · 1

    (B)(4). COVIDIEN IS SUBMITTING THIS REPORT ON BEHALF OF (B)(4), (IMPORTER).

    Description of Event or Problem · 1

    PROCEDURE: STRESS URINARY INCONTINENCE. ACCORDING TO THE REPORTER: THE PATIENT ALLEGED INJURY.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1128 UNK URETEX MESH PRODUCT NONE OTN SOFRADIM PRODUCTION

    Patients

    Seq Age Sex Outcome Treatment
    1 40 YR Other