FDA Adverse Event Malfunction Summary report: N

BD NEXIVA¿ CLOSED IV CATHETER SYSTEM

MDR report key: 17409701 · Received July 27, 2023

Report

Report Number
1710034-2023-00832
Event Type
Malfunction
Date Received
July 27, 2023
Date of Event
June 26, 2023
Report Date
May 1, 2025
Manufacturer
BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.
Product Code
FOZ
UDI-DI
30382903835134
PMA / PMN Number
K183399
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
AS
Reporter Occupation
OTHER HEALTH CARE PROFESSIONAL
Health Professional
Yes

Narratives

Additional Manufacturer Narrative · 0

H6: INVESTIGATION SUMMARY: A PHYSICAL SAMPLE WAS NOT AVAILABLE FOR INVESTIGATION BUT BD WAS PROVIDED WITH TWO PHOTOS OF THE ISSUE FOR EVALUATION. A REVIEW OF THE DEVICE HISTORY RECORD WAS PERFORMED FOR THE REPORTED LOT, 0233529, AND NO QUALITY ISSUES WERE FOUND DURING PRODUCTION. ADDITIONALLY, THE ENGINEER REVIEWED THE DEVICE HISTORY RECORD FOR THE LOT OBSERVED ON THE DEVICES IN THE PICTURES, 1147990, AND NO QUALITY ISSUES WERE FOUND DURING PRODUCTION. OUR QUALITY ENGINEER REVIEWED THE PROVIDED PHOTOS AND OBSERVED IN THE FIRST PHOTO A DISPENSER BOX LABELED AS, "PRODUCT OF MEXICO," WITH A VISIBLE LOT OF 0233529. THE SECOND PHOTO SHOWED THE PRODUCT LABEL OF A 22 GAUGE NEXIVA SINGLE PORT DEVICE FROM LOT 1147990 AND THE MARKING, "MADE IN USA." THIS INDICATED THAT THESE DEVICES WERE MANUFACTURED IN THE USA BUT THE DISPENSER BOX WAS FROM MEXICO. ADDITIONALLY, IT WAS ALSO DETERMINED FROM MANUFACTURING RECORDS THAT LOT 0233529 WAS MADE AT A DIFFERENT PLANT THAN THE DEVICES AND IN 2020 WHILE THE LOT VISIBLE ON THE DEVICE LABEL WAS MADE A YEAR LATER IN 2021 AT A DIFFERENT MANUFACTURING FACILITY. THEREFORE, IT WAS VERY UNLIKELY THAT THE REPORTED ISSUE OCCURRED DURING THE MANUFACTURING/PACKAGING PROCESS OR DURING TRANSIT SINCE EACH DISPENSER AND SHIPPING BOX ARE FILLED BY THEIR MANUFACTURING FACILITY AND WRAPPED PRIOR TO RELEASE. BOTH MANUFACTURING FACILITIES HAVE BEEN NOTIFIED OF THIS INCIDENT AND THE FINDINGS WITH THE VISIBLE LOTS. FINALLY, THE ENGINEER WAS UNABLE TO DETERMINE A DEFINITIVE ROOT CAUSE FOR THE REPORTED ISSUE.

Additional Manufacturer Narrative · 0

H3. A DEVICE EVALUATION IS ANTICIPATED BUT HAS NOT YET BEGUN. UPON COMPLETION OF THE INVESTIGATION, A SUPPLEMENTAL REPORT WILL BE FILED.

Additional Manufacturer Narrative · 0

BECTON DICKINSON AND COMPANY'S (BD) MEDICATION DELIVERY SOLUTIONS (MDS) BUSINESS UNIT WILL DISCONTINUE MALFUNCTION MDR REPORTING FOR CERTAIN DEVICE FAILURES THAT HAVE NOT CAUSED OR CONTRIBUTED TO DEATHS OR SERIOUS INJURIES IN THE PAST TWO YEARS, AND WHERE THE LIKELIHOOD OF A DEATH OR SERIOUS INJURY AS A RESULT OF THESE MALFUNCTIONS IS REMOTE. THIS DECISION FOLLOWS FDA GUIDELINES (MEDICAL DEVICE REPORTING FOR MANUFACTURERS GUIDANCE FOR INDUSTRY AND FOOD AND DRUG ADMINISTRATION STAFF ISSUED NOV 8, 2016, REFERENCE SECTION 2.15). BD NOTIFIED FDA OF THIS DECISION ON MAR 3, 2025. FDA HAS REVIEWED AND RESPONDED TO BD¿S NOTIFICATION (REFERENCE FDA DOCUMENT # (B)(4)) ON MARCH 7, 2025. THIS DOCUMENTATION IS AVAILABLE IN BD DOCUMENT MANAGEMENT SYSTEM (SAP) AS (B)(4). THIS SUPPLEMENTAL MDR IS BEING FILED TO DOCUMENT THAT THE BELOW DEVICE FAILURE WILL NO LONGER BE CONSIDERED A REPORTABLE MALFUNCTION MDR FOR THE PRODUCT FAMILY BELOW: PRODUCT FAMILY: NEXIVA. DEVICE FAILURE: MIXED PRODUCT / LOTS.

Description of Event or Problem · 0

IT WAS REPORTED THAT THE BD NEXIVA¿ CLOSED IV CATHETER SYSTEM SHELF PACK HAD A DIFFERENT PRODUCT IN SHELF PACK THAN LISTED. THE FOLLOWING WAS RECEIVED FROM THE INITITAL REPORTER: VERBATIM: SHELF PACK OF 383513 CONTAINS 383538 LOT NO 1147990. CUSTOMER ALSO USES 383538 AND HAPPY TO KEEP STOCK.

Description of Event or Problem · 0

IT WAS REPORTED THAT THE BD NEXIVA¿ CLOSED IV CATHETER SYSTEM SHELF PACK HAD A DIFFERENT PRODUCT IN SHELF PACK THAN LISTED. THE FOLLOWING WAS RECEIVED FROM THE INITITAL REPORTER: VERBATIM: SHELF PACK OF 383513 CONTAINS 383538 LOT NO 1147990. CUSTOMER ALSO USES 383538 AND HAPPY TO KEEP STOCK.

Description of Event or Problem · 0

NO ADDITIONAL INFORMATION.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1106422 BD NEXIVA¿ CLOSED IV CATHETER SYSTEM INTRAVASCULAR CATHETER FOZ BECTON DICKINSON INFUSION THERAPY SYSTEMS INC. 0233529 30382903835134

Patients

Seq Age Sex Outcome Treatment
1 NA Unknown