BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    MCKESSON BRANDS

    MDR report key: 23476230 · Received November 5, 2025

    Report

    Report Number
    1451040-2025-00102
    Event Type
    Malfunction
    Date Received
    November 5, 2025
    Date of Event
    October 7, 2025
    Report Date
    November 5, 2025
    Manufacturer
    LIFELONG MEDITECH PRIVATE LIMITED
    Product Code
    FMF
    Product Problem
    Yes
    Report Source
    Distributor report
    Reporter Location
    CA, US
    Reporter Occupation
    OTHER HEALTH CARE PROFESSIONAL
    Health Professional
    Yes

    Narratives

    Description of Event or Problem · 0

    IT WAS REPORTED BY THE CUSTOMER THAT WHEN SCREWING THE NEEDLE ON THE SYRINGE, THE NEEDLE POPPED OFF AND MEDICATION LEAKED. NO INFORMATION WAS RECEIVED REGARDING ANY SERIOUS INJURY AS A RESULT OF THESE PRODUCT ISSUES.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    2677803 MCKESSON BRANDS SYRINGE, LL W/O NDL 1CC FMF LIFELONG MEDITECH PRIVATE LIMITED 032501-B

    Patients

    Seq Age Sex Outcome Treatment
    1 NA Unknown