FDA Adverse Event Death Summary report: N

SELECT SECURE

MDR report key: 3122199 · Received May 21, 2013

Report

Report Number
2649622-2013-05419
Event Type
Death
Date Received
May 21, 2013
Date of Event
April 24, 2013
Report Date
April 26, 2013
Manufacturer
MPRI
Product Code
NVY
PMA / PMN Number
P030036
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
UK
Reporter Occupation
PHYSICIAN

Narratives

Additional Manufacturer Narrative · 1

THIS EVENT OCCURRED OUTSIDE THE US WHERE THE SAME MODEL IS DISTRIBUTED. ALL INFORMATION PROVIDED IS INCLUDED IN THIS REPORT. PATIENT INFORMATION IS NOT GENERALLY AVAILABLE DUE TO CONFIDENTIALITY CONCERNS. (B)(4) IMPLANTABLE PULSE GENERATOR (IPG) IMPLANTED (B)(6) 2013; 5076 IMPLANTABLE PACING LEAD IMPLANTED (B)(6) 2013; 5076 IMPLANTABLE PACING LEAD IMPLANTED (B)(6) 2013.

Description of Event or Problem · 1

IT WAS REPORTED THE PATIENT, WHO WAS ENROLLED IN THE (B)(4) STUDY, PRESENTED TO THE EMERGENCY ROOM WITH LEFT SIDED RIB PAIN FIVE DAYS POST IMPLANT OF THE IMPLANTABLE PULSE GENERATOR (IPG) SYSTEM. A CHEST XRAY SHOWED BLUNTING OF THE COSTOPHRENIC ANGLE AND THE PATIENT WAS ADMITTED FOR OBSERVATION. A REPEAT CHEST X-RAY TWO DAYS LATER NOTED A ¿WHITE OUT ON THE LEFT LUNG FIELD.¿ A NEEDLE ASPIRATION CONFIRMED A HEMOTHORAX. THE PATIENT IS REPORTED TO HAVE HAD A CARDIAC ARREST WITH UNSUCCESSFUL RESUSCITATION AND DIED. ADDITIONAL INFORMATION RECEIVED NOTED THAT NO BLOOD WAS PRESENT IN THE PERICARDIUM AND THAT HEMOTHORAX WAS ¿MOST LIKELY¿ CAUSED BY CONTINUED OOZING FROM SUBCLAVIAN INSERTION SITE FOLLOWED BY DETERIORATION ASSOCIATED WITH ANTIBIOTIC CAUSING AN INCREASED INR LEVEL. THE CAUSE OF DEATH WAS REPORTED AS CARDIAC ENLARGEMENT, LEFT HEMOTHORAX FOLLOWING RECENT PACER INSERTION.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
223686 SELECT SECURE DRUG-ELUTING PERMANENT DEFIBRILLATOR ELECTRODES NVY MPRI 383098

Patients

Seq Age Sex Outcome Treatment
1 00072 YR Death| H| L| R