BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    J & J STENT

    MDR report key: 31486 · Received January 30, 1996

    Report

    Report Number
    31486
    Event Type
    Malfunction
    Date Received
    January 30, 1996
    Report Date
    August 1, 1995
    Manufacturer
    JOHNSON & JOHNSON INTERVENTIONAL SYSTEMS CO.
    Product Code
    MAF
    Product Problem
    Yes
    Report Source
    User Facility report
    Reporter Location
    PA, US
    Reporter Occupation
    RISK MANAGER

    Narratives

    Description of Event or Problem · 1

    STENT DISCONNECTED FROM CATHETER. LOST IN VASCULATURE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 J & J STENT STENT MAF JOHNSON & JOHNSON INTERVENTIONAL SYSTEMS CO. HH0379

    Patients

    Seq Age Sex Outcome Treatment
    1 NO INFO