FDA Adverse Event Malfunction Summary report: N

TITANIUM GREENFIELD VENA CAVA FILTER

MDR report key: 296859 · Received September 19, 2000

Report

Report Number
6000036-2000-00076
Event Type
Malfunction
Date Received
September 19, 2000
Date of Event
August 17, 2000
Report Date
August 21, 2000
Manufacturer
MEDI-TECH / A DIV OF BOSTON SCIENTIFIC CORP.
Product Code
DTK
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
TN, US
Reporter Occupation
PHYSICIAN

Narratives

Description of Event or Problem · 1

IT WAS REPORTED FOLLOWING AN INCOMPLETE OPENING OF ANOTHER FILTER, THIS FILTER WAS THEN DEPLOYED VIA A JUGULAR APPROACH AND ALSO DID NOT APPEAR TO OPEN COMPLETELY. MANIPULATION ATTEMPTS WITH A DILATOR AND A "J" TIP STYLE GUIDEWIRE WERE UNSUCCESSFUL IN ACHIEVING A COMPLETE OPENING. THE PHYSICIAN FEELS THE PT IS PROTECTED AND A THIRD FILTER WAS NOT PLACED. THIS DEVICE REMAINS IMPLANTED. THEREFORE, NO FAILURE ANALYSIS WILL BE AVAILABLE. F/U INDICATED CONTINUAL FLUSHING OF THE CARRIER SYSTEM DURING THE IMPLANT PROCEDURE WAS NOT PERFORMED WHICH CO BELIEVES MAY HAVE CONTRIBUTED TO THIS EVENT. HOWEVER, CO IS UNABLE TO DETERMINE THE EXACT CAUSE FOR THIS EVENT. DIRECTIONS FOR USE: "DO NOT ATTEMPT TO MOVE OR MANIPULATE AN ENGAGED FILTER... IN MOST CASES, A SECOND FILTER, PROPERLY PLACED, SHOULD BE IMPLANTED FOR PROTECTION AGAINST RECURRENT 'PE'... THE INTRODUCER CATHETER MUST BE FLUSHED THROUGH THE FLUSH PORT BY FREQUENT INJECTION OR CONTINUOUS INFUSION OF STERILE HEPARINIZED SALINE DURING THE IMPLANT PROCEDURE... INSUFFICIENT FLUSHING CAN ALLOW THROMBUS FORMATION INSIDE THE TITANIUM GREENFIELD VENA CAVA FILTER WHICH CAN BIND THE LEGS AND PREVENT COMPLETE OPENING UPON RELEASE... SAME CASE AS MFR REPORT# 6000036-2000-00078.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 TITANIUM GREENFIELD VENA CAVA FILTER VENA CAVA FILTER DTK MEDI-TECH / A DIV OF BOSTON SCIENTIFIC CORP. NA 3147576

Patients

Seq Age Sex Outcome Treatment
1 UNKNOWN