BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    MCKESSON BRANDS

    MDR report key: 24506160 · Received March 4, 2026

    Report

    Report Number
    1451040-2026-00015
    Event Type
    Malfunction
    Date Received
    March 4, 2026
    Date of Event
    February 25, 2026
    Report Date
    March 4, 2026
    Manufacturer
    LIFELONG MEDITECH PRIVATE LIMITED
    Product Code
    FMF
    UDI-DI
    10612479207001
    Product Problem
    Yes
    Report Source
    Distributor report
    Reporter Location
    MT, US
    Reporter Occupation
    OTHER HEALTH CARE PROFESSIONAL
    Health Professional
    Yes

    Narratives

    Description of Event or Problem · 0

    IT WAS REPORTED BY THE CUSTOMER THAT SYRINGES ARE CRACKED ON THE SIDES AND THE MEDICINE IS COMING THROUGH THE SIDES.

    Devices

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

    Patients

    Seq Age Sex Outcome Treatment
    1 NA Unknown