BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    MCKESSON BRANDS

    MDR report key: 23335579 · Received October 20, 2025

    Report

    Report Number
    1451041-2025-00098
    Event Type
    Malfunction
    Date Received
    October 20, 2025
    Date of Event
    October 10, 2025
    Report Date
    October 20, 2025
    Manufacturer
    HARSORIA HEALTHCARE
    Product Code
    QOI
    UDI-DI
    10612479268583
    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

    IT WAS REPORTED BY THE CUSTOMER THAT SOME OF THE NEEDLES DO NOT RETRACT COMPLETELY. 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
    298091 MCKESSON BRANDS CATH, IV SFTY WNGD PUSH BUTTONBLU 22GX1" QOI HARSORIA HEALTHCARE 40885/0517 10612479268583

    Patients

    Seq Age Sex Outcome Treatment
    1 NA Unknown