BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    MCKESSON BRAND

    MDR report key: 23552186 · Received November 14, 2025

    Report

    Report Number
    1451040-2025-00105
    Event Type
    Malfunction
    Date Received
    November 14, 2025
    Date of Event
    October 16, 2025
    Report Date
    November 14, 2025
    Manufacturer
    LIFELONG MEDITECH PRIVATE LIMITED
    Product Code
    FMF
    UDI-DI
    10612479207001
    Product Problem
    Yes
    Report Source
    Distributor report
    Reporter Location
    VA, US
    Reporter Occupation
    OTHER HEALTH CARE PROFESSIONAL
    Health Professional
    Yes

    Narratives

    Description of Event or Problem · 0

    THE CUSTOMER REPORTED THAT THEY WERE HAVING DIFFICULTY WITH THE SYRINGE. THE LUER LOCK IS DEFECTIVE AND SPRAYING OUT OF THE TIP OF THE SYRINGE DURING AN INJECTION. NO INFORMATION WAS RECEIVED REGARDING ANY SERIOUS INJURY AS A RESULT OF THIS PRODUCT ISSUE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1984953 MCKESSON BRAND SYRINGE, LL 5CC FMF LIFELONG MEDITECH PRIVATE LIMITED 042505-D 10612479207001

    Patients

    Seq Age Sex Outcome Treatment
    1 NA Unknown