FDA Adverse Event Death Summary report: N

ATTAIN ABILITY

MDR report key: 2061609 · Received April 18, 2011

Report

Report Number
2649622-2011-07194
Event Type
Death
Date Received
April 18, 2011
Date of Event
March 19, 2011
Manufacturer
MEDTRONIC PUERTO RICO, INC.
Product Code
OJX
PMA / PMN Number
P080006
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.

Description of Event or Problem · 1

IT WAS REPORTED THAT THE PATIENT DIED APPROXIMATELY FOUR MONTHS AFTER AN UPGRADE TO A BI-VENTRICULAR IMPLANTABLE CARDIAC DEFIBRILLATOR SYSTEM. CAUSE OF DEATH IS NOT DETERMINED, BUT NOTED TO BE POSSIBLE MYOCARDIAL INFARCTION. NO AUTOPSY PERFORMED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 ATTAIN ABILITY IMPLANTABLE PACING LEAD OJX MEDTRONIC PUERTO RICO, INC. 4196 ASKU

Patients

Seq Age Sex Outcome Treatment
1 57 YR Death