BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    INNOVATIVE MEDICAL TECHNOLOGIES INC.

    MDR report key: 25048273 · Received April 30, 2026

    Report

    Report Number
    3001451226-2026-00001
    Event Type
    Malfunction
    Date Received
    April 30, 2026
    Date of Event
    March 20, 2026
    Report Date
    April 30, 2026
    Manufacturer
    INNOVATIVE MEDICAL TECHNOLOGIES
    Product Code
    JKA
    UDI-DI
    00857182006487
    PMA / PMN Number
    K220458
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    MN, US
    Reporter Occupation
    OTHER HEALTH CARE PROFESSIONAL
    Health Professional
    Yes

    Narratives

    Additional Manufacturer Narrative · 0

    COULD NOT REPRODUCE PROBLEM DURING TESTING.

    Description of Event or Problem · 0

    BUTTERFLY NEEDLE DID NOT RETRACT FULLY INTO THE SHEATH WHEN BUTTON WAS PUSHED.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    190745 INNOVATIVE MEDICAL TECHNOLOGIES INC. PUSH BUTTON BLOOD COLLECTION SET JKA INNOVATIVE MEDICAL TECHNOLOGIES 250402M 00857182006487

    Patients

    Seq Age Sex Outcome Treatment
    1