FDA Adverse Event Malfunction Summary report: N

BD TEXIUM CLOSED MALE LUER WITH FEMALE CAP

MDR report key: 23295248 · Received October 15, 2025

Report

Report Number
9616066-2025-03092
Event Type
Malfunction
Date Received
October 15, 2025
Date of Event
September 18, 2025
Report Date
January 13, 2026
Manufacturer
SISTEMAS MEDICOS ALARIS S.A DE C.V.
Product Code
FPA
UDI-DI
10885403221705
PMA / PMN Number
K053049
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
NJ, US
Reporter Occupation
OTHER HEALTH CARE PROFESSIONAL
Health Professional
Yes

Narratives

Additional Manufacturer Narrative · 0

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

Additional Manufacturer Narrative · 0

THREE PHOTOS WERE RECEIVED FOR QUALITY EVALUATION. EXAMINATION OF THE PHOTOS SHOW THAT THERE IS LEAKAGE AT THE CONNECTION POINT BETWEEN THE TEXIUM CONNECTOR AND A BD SMARTSITE CONNECTION POINT. THE CUSTOMER COMPLAINT OF LEAKAGE WAS CONFIRMED. A TREND HAS BEEN IDENTIFIED, AND ACTIONS HAVE BEEN INITIATED TO INVESTIGATE THE ISSUE. CORRECTIVE ACTIONS TAKEN DURING THIS INVESTIGATION WILL BE IMPLEMENTED IN OUR PRODUCTION PROCESS TO FURTHER INCREASE THE ROBUSTNESS AND RELIABILITY OF THE DEVICE AND PREVENT FUTURE OCCURRENCES OF THIS TYPE. A DEVICE HISTORY RECORD REVIEW FOR MODEL 10012241-0500 LOT NUMBER 24095556 WAS PERFORMED. THERE WERE NO QUALITY NOTIFICATIONS ISSUED FOR THE FAILURE MODE REPORTED BY THE CUSTOMER DURING THE PRODUCTION BUILD OF THIS SET.

Description of Event or Problem · 0

IT WAS REPORTED THAT THE BD TEXIUM CLOSED MALE LUER WITH FEMALE CAP HAD LEAKAGE. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: UMC LUBBOCK HAS EXPERIENCED SEVERAL TEXIUM LEAKS - STANDALONE AND BONDED - WHILE INFUSING CHEMO / HD.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
2536957 BD TEXIUM CLOSED MALE LUER WITH FEMALE CAP INTRAVASCULAR ADMINISTRATION SET FPA SISTEMAS MEDICOS ALARIS S.A DE C.V. 25025394 10885403221705

Patients

Seq Age Sex Outcome Treatment
1 NA Unknown