BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    EMBECTA SYRINGE

    MDR report key: 24160627 · Received January 23, 2026

    Report

    Report Number
    24160627
    Event Type
    Malfunction
    Date Received
    January 23, 2026
    Date of Event
    December 19, 2025
    Report Date
    December 19, 2025
    Manufacturer
    EMBECTA MEDICAL II LLC
    Product Code
    FMF
    Product Problem
    Yes
    Report Source
    User Facility report
    Reporter Location
    MN
    Reporter Occupation
    OTHER HEALTH CARE PROFESSIONAL
    Health Professional
    Yes

    Narratives

    Description of Event or Problem · 0

    RN ADMINISTERING INSULIN SQ [SUB-CUTANEOUS] TO PATIENT. NEEDLE DID NOT SELF-RETRACT. NEEDLE STICK INJURY TO WRITER.

    Description of Event or Problem · 0

    RN ADMINISTERING INSULIN SQ [SUB-CUTANEOUS] TO PATIENT. NEEDLE DID NOT SELF-RETRACT. NEEDLE STICK INJURY TO WRITER.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    220378 EMBECTA SYRINGE SYRINGE, PISTON FMF EMBECTA MEDICAL II LLC 4311022

    Patients

    Seq Age Sex Outcome Treatment
    1 NA Unknown