BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    MAXZERO NEEDLELESS CONNECTOR

    MDR report key: 22726800 · Received August 6, 2025

    Report

    Report Number
    22726800
    Event Type
    Malfunction
    Date Received
    August 6, 2025
    Date of Event
    July 19, 2025
    Report Date
    July 21, 2025
    Manufacturer
    BD SWITZERLAND SÀRL
    Product Code
    FPA
    Product Problem
    Yes
    Report Source
    User Facility report
    Reporter Location
    PA
    Reporter Occupation
    OTHER HEALTH CARE PROFESSIONAL
    Health Professional
    Yes

    Narratives

    Description of Event or Problem · 0

    PRODUCT ISSUE: WHILE DISCONNECTING THE BLUE VACUTAINER TRANSFER DEVICE FROM A CVAD [CENTRAL VENOUS ACCESS DEVICE] WITH A BD MAXZERO NEEDLELESS CONNECTOR, THE CONNECTOR SHOT OUT 2 DROPLETS OF BLOOD ONTO MY FACE WITHIN A 1/2 INCH OF MY EYE. I WASHED MY FACE WITH SOAP AND WATER. I OVERHEARD THAT THIS IS A COMMON ISSUE OF FLUIDS COMING OUT OF THE CONNECTOR LIKE THIS. PRODUCT INFORMATION: BD MAXZERO NEEDLELESS CONNECTOR, LOT 1025055304, EXP DATE 2028-05-13.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    1528172 MAXZERO NEEDLELESS CONNECTOR SET, ADMINISTRATION, INTRAVASCULAR FPA BD SWITZERLAND SÀRL 1025055304

    Patients

    Seq Age Sex Outcome Treatment
    1 77 YR Male