BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    MCKESSON BRANDS

    MDR report key: 23764604 · Received December 9, 2025

    Report

    Report Number
    1451040-2025-00119
    Event Type
    Malfunction
    Date Received
    December 9, 2025
    Date of Event
    November 17, 2025
    Report Date
    December 9, 2025
    Manufacturer
    LIFELONG MEDITECH PRIVATE LIMITED
    Product Code
    FMF
    UDI-DI
    20612479273218
    Product Problem
    Yes
    Report Source
    Distributor report
    Reporter Location
    AZ, US
    Reporter Occupation
    OTHER HEALTH CARE PROFESSIONAL
    Health Professional
    Yes

    Narratives

    Description of Event or Problem · 0

    IT WAS REPORTED BY THE CUSTOMER THAT 2 SYRINGES HAVE HAD THE LUER LOCK TIP COME OFF DURING USE. 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
    1990407 MCKESSON BRANDS SYRINGE, LL 60CC FMF LIFELONG MEDITECH PRIVATE LIMITED 042560-E 20612479273218

    Patients

    Seq Age Sex Outcome Treatment
    1 NA Unknown