FDA Adverse Event Malfunction Summary report: N

BD INTIMA-II¿ IV CATHETER

MDR report key: 15276862 · Received August 23, 2022

Report

Report Number
3014704491-2022-00371
Event Type
Malfunction
Date Received
August 23, 2022
Date of Event
July 8, 2022
Report Date
August 9, 2022
Manufacturer
BD (SUZHOU)
Product Code
FOZ
PMA / PMN Number
NA
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
CH
Reporter Occupation
OTHER HEALTH CARE PROFESSIONAL
Health Professional
Yes

Narratives

Additional Manufacturer Narrative · 0

INVESTIGATION SUMMARY: IN RESPONSE TO THE EVENT REPORTED BY THE FACILITY A DEVICE HISTORY REVIEW WAS CONDUCTED FOR LOT NUMBER 1230637. 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. BASED ON THE DESCRIPTION OF THE EVENT, OUR ENGINEERS WERE ABLE TO DETERMINE THAT THE MOST LIKELY ROOT CAUSE FOR THIS EVENT IS THE FORCING OF FLUID THROUGH THE DEVICE DURING INJECTION. THE BD INTIMA-II IS AN INFUSION ONLY DEVICE AND IS NOT RATED FOR HIGH PRESSURE INJECTIONS. BD ENCOURAGES THE REVIEW OF THE INSTRUCTIONS FOR USE INCLUDED WITH ALL INTIMA-II UNITS; BD WILL CONTINUE TO TRACK AND TREND FOR THIS ISSUE.

Description of Event or Problem · 0

IT WAS REPORTED THAT THE BD INTIMA-II¿ IV CATHETER EXPERIENCED LEAKAGE AT THE CONNECTION SITE. THE FOLLOWING INFORMATION WAS PROVIDED BY THE INITIAL REPORTER: THE INDWELLING NEEDLE WAS CLAMPED BEFORE THE PLACEMENT OF THE PATIENT, AND OPENED AFTER THE PLACEMENT WAS COMPLETED. FLUID LEAKAGE AND BLOOD LEAKAGE WERE FOUND AT THE CLAMP PART OF INDWELLING NEEDLE .

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
2822240 BD INTIMA-II¿ IV CATHETER INTRAVASCULAR CATHETER FOZ BD (SUZHOU) 1230637

Patients

Seq Age Sex Outcome Treatment
1 Unknown