BEUDAMED
    FDA Adverse Event Malfunction Summary report: N

    SAF-T-INTIMA Y ADP YEL 24GA X 0.75IN

    MDR report key: 24402415 · Received February 20, 2026

    Report

    Report Number
    3006948883-2026-00150
    Event Type
    Malfunction
    Date Received
    February 20, 2026
    Date of Event
    February 5, 2026
    Report Date
    March 13, 2026
    Manufacturer
    BD SUZHOU (MDS)
    Product Code
    FOZ
    PMA / PMN Number
    UNK
    Product Problem
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    NL
    Reporter Occupation
    OTHER HEALTH CARE PROFESSIONAL
    Health Professional
    Yes

    Narratives

    Additional Manufacturer Narrative · 0

    INVESTIGATION RESULTS: A DEVICE HISTORY REVIEW WAS CONDUCTED FOR LOT NUMBER 5162992. OUR RECORDS SHOW THAT THIS IS THE ONLY INSTANCE OF THIS ISSUE OCCURRING IN THIS PRODUCTION BATCH. ACCORDING TO THE SAMPLING PLAN APPLIED FOR PRODUCT PERFORMANCE, THIS LOT WAS ACCEPTED AND RELEASED WITHOUT DEFECTS BEING NOTED DURING THE FINAL ASSEMBLY OR VISUAL INSPECTIONS. A SAMPLE COULD NOT BE OBTAINED FOR EVALUATION AND TESTING; IN LIEU OF THE AFFECTED DEVICE, FUNCTIONAL TESTING WAS PERFORMED ON RETENTION SAMPLES FOR THIS LOT, THE RESULTS OF THESE SHOW THAT THE TESTED UNITS PERFORMED WITHIN PRODUCT SPECIFICATIONS. UNFORTUNATELY, WITHOUT THE ABILITY TO INVESTIGATE THE AFFECTED UNIT OUR QUALITY ENGINEERS WERE UNABLE TO DETERMINE THE ROOT CAUSE FOR THIS COMPLAINT. BD WILL CONTINUE TO MONITOR THIS ISSUE.

    Additional Manufacturer Narrative · 0

    H.3. IF A DEVICE EVALUATION AND/OR DEVICE HISTORY REVIEW IS COMPLETED, A SUPPLEMENTAL REPORT WILL BE FILED.

    Description of Event or Problem · 0

    NO ADDITIONAL INFORMATION.

    Description of Event or Problem · 0

    IT WAS REPORTED THAT AFTER INSERTING THE BUTTERFLY NEEDLE, THE SAFETY SLEEVE REMAINS IN PLACE. AFTER INSERTING THE BUTTERFLY NEEDLE, THE SAFETY SLEEVE REMAINS IN PLACE. THE NEEDLE IS REMOVED WITHOUT THE SAFETY SLEEVE. REMOVING THE NEEDLE WAS LABORIOUS. WHEN DID THE INCIDENT OCCUR? - BEFORE USE.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    181166 SAF-T-INTIMA Y ADP YEL 24GA X 0.75IN INTRAVASCULAR CATHETER FOZ BD SUZHOU (MDS) 5162992

    Patients

    Seq Age Sex Outcome Treatment
    1 NA Unknown