FDA Adverse Event Death Summary report: N

CAPSUREFIX NOVUS

MDR report key: 1972034 · Received January 27, 2011

Report

Report Number
2649622-2011-00137
Event Type
Death
Date Received
January 27, 2011
Date of Event
August 15, 2010
Manufacturer
MEDTRONIC PUERTO RICO, INC.
Product Code
DTB
PMA / PMN Number
P930039/S009
Removal / Correction Number
ASKU
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

THE INFORMATION SUBMITTED REFLECTS ALL RELEVANT DATA RECEIVED. IF ADDITIONAL RELEVANT INFORMATION IS RECEIVED, A SUPPLEMENTAL REPORT WILL BE SUBMITTED.

Additional Manufacturer Narrative · 1

ADDITIONAL INFORMATION RECEIVED INDICATED THAT THE PATIENT WAS UNRESPONSIVE AND EMERGENCY MEDICAL SERVICES WERE CALLED AND CARDIOPULMONARY RESUSCITATION (CPR) WAS INITIATED. THE INITIAL RHYTHM WAS VENTRICULAR FIBRILLATION THAT WAS DEFIBRILLATED FIVE TIMES TO PULSELESS ELECTRICAL ACTIVITY. THE PATIENT WAS TRANSPORTED TO THE EMERGENCY ROOM WITH NO PULSE OR RESPIRATIONS, AND REMAINED IN PULSELESS ELECTRICAL ACTIVITY. CPR WAS TERMINATED FOURTEEN MINUTES AFTER ARRIVAL TO THE ER AND THE PATIENT WAS PRONOUNCED DEAD. THE PHYSICIAN INDICATED THE CAUSE OF DEATH WAS MOST LIKELY ADVANCED ATHEROSCLEROTIC CORONARY ARTERY DISEASE. THE INFORMATION SUBMITTED REFLECTS ALL RELEVANT DATA RECEIVED. IF ADDITIONAL RELEVANT INFORMATION IS RECEIVED, A SUPPLEMENTAL REPORT WILL BE SUBMITTED.

Description of Event or Problem · 1

IT WAS NOTED THE PATIENT DIED APPROXIMATELY 8 MONTHS AFTER DEVICE IMPLANT. THE CAUSE OF DEATH HAS BEEN REQUESTED AND NOT RECEIVED.

Description of Event or Problem · 1

IT WAS NOTED THE PATIENT DIED APPROXIMATELY (B)(6) AFTER DEVICE IMPLANT. THE CAUSE OF DEATH HAS BEEN REQUESTED AND NOT RECEIVED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 CAPSUREFIX NOVUS IMPLANTABLE PACING LEAD DTB MEDTRONIC PUERTO RICO, INC. 5076 ASKU

Patients

Seq Age Sex Outcome Treatment
1 78 YR Death