FDA Adverse Event Death Summary report: N

CRONUS ENDOVASCULAR FLOPPY GUIDEWIRE

MDR report key: 493461 · Received October 21, 2003

Report

Report Number
3003778388-2003-00003
Event Type
Death
Date Received
October 21, 2003
Date of Event
August 1, 2003
Report Date
August 1, 2003
Manufacturer
STEREOTAXIS, INC.
Product Code
DQX
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
GM
Reporter Occupation
PHYSICIAN

Narratives

Description of Event or Problem · 1

DURING A CORONARY ARTERY TREATMENT PROCEDURE ATTEMPTS TO CROSS THE LESION IN THE FIRST MARGINAL WITH THE STEREOTAXIS CRONUS ENDOVASCULAR GUIDEWIRE WAS UNSUCCESSFUL. THE CRONUS FLOPPY GUIDEWIRE WAS THEN INSERTED INTO THE LEFT MAIN CORONARY ARTERY. ANGIOGRAPHY REVEALED A PROXIMAL TOTAL OCCLUSION OF THE DOMINANT CIRCUMFLEX ARTERY AND A DISSECTION OF THE PROXIMAL LAD. THE STEREOTAXIS CRONUS FLOPPY WIRE WAS REMOVED AND A COMPETITOR'S WIRE INSERTED. IMMEDIATE RECANALIZATION WAS PERFORMED AND 2 STENTS IMPLANTED. THE CIRCUMFLEX ARTERY REMAINED OPEN BUT WITH A MARKED PERIPHERAL DISSECTION. A COMPETITOR'S GUIDEWIRE WAS THEN ADVANCED INTO THE PERIPHERAL LAD, AND AFTER PREDILATION, THREE STENTS WERE IMPLANTED. AT THE END OF THE PROCEDURE, THE LAD AND CIRCUMFLEX ARTERIES APPEARED OPEN, BUT WITH MARKED DISSECTIONS. AS THE HEMODYNAMIC SITUATION DETERIORATED DURING THE PROCEDURE AND COULD ONLY BE POORLY STABLIZED, IT WAS NECESSARY TO RESUSCITATE THE PATIENT. AN EMERGENCY CORONARY ARTERY BYPASS OPERATION WAS PERFORMED. THE PATIENT RECEIVED TWO SAPHENOUS VEIN BYPASS GRAFTS (LAD AND CIRCUMFLEX). HOWEVER, ATTEMPTS TO WEAN THE PATIENT FROM THE EXTRACORPORAL CIRCULATION FAILED THREE TIMES AND FINALLY THE PATIENT DIED 6 HOURS LATER.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 CRONUS ENDOVASCULAR FLOPPY GUIDEWIRE CORONARY GUIDEWIRE DQX STEREOTAXIS, INC. 001-001096-4 0212-4014

Patients

Seq Age Sex Outcome Treatment
1 * Death| R