BEUDAMED
    FDA Adverse Event Injury Summary report: N

    SHARPS CONTAINER

    MDR report key: 15717 · Received September 1, 1994

    Report

    Report Number
    MW1003249
    Event Type
    Injury
    Date Received
    September 1, 1994
    Date of Event
    July 1, 1994
    Manufacturer
    SAGE PRODUCTS, INC.
    Product Code
    MMK
    Product Problem
    Yes
    Report Source
    Voluntary report
    Reporter Occupation
    NURSE

    Narratives

    Description of Event or Problem · 1

    SAGE PRODUCTS, INC. 815 TEK DR, PO BOX 9693, CRYSTAL LAKE, IL 60014-9693. REGRETFULLY, THE INFO PROVIDED TO US ON THE VOLUNTARY REPORT IS NOT SUFFICIENT FOR US TO LOCATE IF A REPORT WAS MADE TO US. THEREFORE, IT IS IMPOSSIBLE TO EVALUATE IF THERE IS A PRODUCT PROBLEM.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1 SHARPS CONTAINER MMK SAGE PRODUCTS, INC. ALL LOT #S

    Patients

    Seq Age Sex Outcome Treatment
    1 * Required Intervention