BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    MCKESSON BRANDS

    MDR report key: 24201873 · Received January 28, 2026

    Report

    Report Number
    1451040-2026-00006
    Event Type
    Malfunction
    Date Received
    January 28, 2026
    Date of Event
    January 7, 2026
    Report Date
    January 28, 2026
    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 DRAWING MEDICATIONS, SYRINGES ARE LEAKING AND ARE HARD TO PUSH. 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
    259982 MCKESSON BRANDS SYRINGE, LL W/O NDL 1CC FMF LIFELONG MEDITECH PRIVATE LIMITED UNKNOWN

    Patients

    Seq Age Sex Outcome Treatment
    1 NA Unknown