BEUDAMED
    FDA Adverse Event Injury Summary report: N

    INTERSTIM II

    MDR report key: 1980299 · Received February 2, 2011

    Report

    Report Number
    3004209178-2011-00817
    Event Type
    Injury
    Date Received
    February 2, 2011
    Date of Event
    January 27, 2011
    Report Date
    January 27, 2011
    Manufacturer
    MDT PUERTO RICO OPERATIONS CO., JUNCOS
    Product Code
    EZW
    PMA / PMN Number
    P970004
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    IN, US
    Reporter Occupation
    PHYSICIAN

    Narratives

    Additional Manufacturer Narrative · 1

    (B)(4).

    Description of Event or Problem · 1

    IT WAS REPORTED THAT THE PATIENT HAS HAD DEVICE INFECTIONS OFF AND ON SINCE IMPLANT. THE PT REPORTEDLY WAS DIAGNOSED WITH (B)(6). THE PHYSICIAN PLANNED TO REMOVE THE DEVICE SYSTEM ON (B)(6) 2011. ADD'L INFO WAS REQUESTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 INTERSTIM II EZW MDT PUERTO RICO OPERATIONS CO., JUNCOS 3058 NA

    Patients

    Seq Age Sex Outcome Treatment
    1 Required Intervention PROGRAMMER: MODEL 3037, LOT# NJD113312N| IMPLANTED:| EXPLANTED:| LEAD: MODEL 3889, LOT# V519077