BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    SHARPS CONTAINER

    MDR report key: 24059764 · Received January 13, 2026

    Report

    Report Number
    3003674698-2026-00182
    Event Type
    Malfunction
    Date Received
    January 13, 2026
    Product Code
    MMK
    UDI-DI
    00816703021392
    PMA / PMN Number
    K180984
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    MN, US
    Reporter Occupation
    OTHER

    Narratives

    Description of Event or Problem · 0

    SHARPS DART LOCKING MECHANISM DOES NOT REMAIN PERMANENTLY LOCKED. PART AND LOT NUMBERS INVOLVED: MS-64250 - 1011735 AND 1012015. 64250 - 1011532, 1011528, 1011581, 1011585, 1011955, 1011967, 1012051, AND 1012206.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    113546 SHARPS CONTAINER MMK MS-64250, 64250 00816703021392

    Patients

    Seq Age Sex Outcome Treatment
    1 NA Unknown