FDA Adverse Event Malfunction Summary report: N

CODMAN BEVD 1.9MM CAT SET

MDR report key: 21858504 · Received April 17, 2025

Report

Report Number
3013886523-2025-00077
Event Type
Malfunction
Date Received
April 17, 2025
Date of Event
March 6, 2025
Report Date
June 13, 2025
Manufacturer
INTEGRA LIFESCIENCES MANSFIELD
Product Code
JXG
UDI-DI
10381780518440
PMA / PMN Number
K233448
Product Problem
Yes
Report Source
Manufacturer report
Reporter Occupation
OTHER
Health Professional
N

Narratives

Additional Manufacturer Narrative · 0

UPDATED FIELDS: D4, D9, G3, G6, H2, H3, H4, H6, H11. THE BACTISEAL CATHETER (ID 821749) WAS RETURNED FOR EVALUATION. DEVICE HISTORY RECORD (DHR) - THE PRODUCT CODE 821749 WITH LOT 7365500, CONFORMED TO THE SPECIFICATIONS WHEN RELEASED TO STOCK. FAILURE ANALYSIS - THE CATHETER WAS VISUALLY INSPECTED. THE LEAK TEST WAS PERFORMED; A LEAK WAS NOTED. THE COMPLAINT WAS CONFIRMED. ROOT CAUSE ANALYSIS - A POSSIBLE ROOT CAUSE FOR THE ISSUE REPORTED BY THE CUSTOMER, COULD BE DUE TO A SHARP OR POINTED OBJECT COMING INTO CONTACT WITH THE CATHETER, AS NOTED IN THE IFU SILICONE HAS A LOW CUT/TEAR RESISTANCE.

Additional Manufacturer Narrative · 0

AN INVESTIGATION HAS BEEN INITIATED BASED ON THE REPORTED INFORMATION. UPON COMPLETION OF THE INVESTIGATION, A FOLLOW-UP REPORT WILL BE SUBMITTED.

Description of Event or Problem · 0

NA.

Description of Event or Problem · 0

A FACILITY REPORTED A BACTISEAL CATHETER (ID (B)(4) WAS LEAKING A MINIMAL AMOUNT OF CEREBROSPINAL FLUID (CSF) AT THE SIDE WALL OF THE END PORTION OF THE CATHETER. THE EVENT HAPPENED DURING IMPLANTATION (BEFORE IMPLANTATION SITE CLOSURE). THE PROCEDURE WAS COMPLETED WITH A REPLACEMENT PRODUCT AVAILABLE. NO ADVERSE CONSEQUENCES REPORTED, AND THE EVENT DID NOT LED TO SURGICAL DELAY.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1776773 CODMAN BEVD 1.9MM CAT SET BACTISEAL EVD CATHETERS JXG INTEGRA LIFESCIENCES MANSFIELD 7365500 10381780518440

Patients

Seq Age Sex Outcome Treatment
1 NA Unknown