BEUDAMED
    FDA Adverse Event Injury Summary report: N

    SWIFT-LOCK ANCHOR

    MDR report key: 7637777 · Received June 26, 2018

    Report

    Report Number
    1627487-2018-05961
    Event Type
    Injury
    Date Received
    June 26, 2018
    Report Date
    June 26, 2018
    Manufacturer
    ST. JUDE MEDICAL - NEUROMODULATION
    Product Code
    GZB
    UDI-DI
    05415067024084
    PMA / PMN Number
    K092371
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    AZ, US
    Reporter Occupation
    PHYSICIAN

    Narratives

    Additional Manufacturer Narrative · 1

    IN THE EVENT THE DEVICE IS RETURNED TO THE MANUFACTURER, THE REPORTED EVENT CANNOT BE ANALYZED VIA LABORATORY TESTING. MANUFACTURER HAS LIMITED INFORMATION RELATED TO THE PATIENT'S MEDICAL HISTORY AND IS UNABLE TO FORM AN OPINION AS TO THE RELEVANCY OF THE PATIENT'S HISTORY TO THE EVENT REPORTED. MANUFACTURER DEFERS TO THE PATIENT'S PHYSICIAN REGARDING MEDICAL HISTORY.

    Description of Event or Problem · 1

    DEVICE 4 OF 5. REFERENCE MFR. REPORT# 1627487-2018-05958. REFERENCE MFR. REPORT# 3006705815-2018-01468. REFERENCE MFR. REPORT# 3006705815-2018-01469. REFERENCE MFR. REPORT# 1627487-2018-05962. IT WAS REPORTED THE PHYSICIAN INDICATED A POSSIBLE INFECTION AROUND THE IPG AND LEADS SITE. THE PATIENT WAS PRESCRIBED ANTIBIOTICS. CULTURES PRESUMED NEGATIVE FOR AN INFECTION. IN TURN, THE ENTIRE SYSTEM WAS EXPLANTED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    480401 SWIFT-LOCK ANCHOR SCS ANCHOR GZB ST. JUDE MEDICAL - NEUROMODULATION 1192 6242827 05415067024084

    Patients

    Seq Age Sex Outcome Treatment
    1 Other