BEUDAMED
    FDA Adverse Event Injury Summary report: N

    VETRIJET

    MDR report key: 24646152 · Received March 19, 2026

    Report

    Report Number
    1000138447-2026-00002
    Event Type
    Injury
    Date Received
    March 19, 2026
    Date of Event
    February 10, 2026
    Report Date
    March 19, 2026
    Manufacturer
    HLB LIFE SCIENCE CO. LTD.
    Product Code
    FMF
    Adverse Event
    Yes
    Product Problem
    Yes
    Report Source
    Distributor report
    Reporter Location
    WA, US
    Reporter Occupation
    OTHER HEALTH CARE PROFESSIONAL
    Health Professional
    Yes

    Narratives

    Description of Event or Problem · 0

    TECHNICIAN RECEIVED A LIGHT STAB WHEN SHE REACHED INTO A DRAWER FOR AN ITEM FROM A NEEDLE THAT WAS STILL PACKAGED BUT DID NOT HAVE A PROTECTIVE CAP.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    201719 VETRIJET SYRINGE FMF HLB LIFE SCIENCE CO. LTD. 670231 250901

    Patients

    Seq Age Sex Outcome Treatment
    1 NA Unknown