FDA Adverse Event Death Summary report: N

CURRENT RF DR

MDR report key: 1010874 · Received March 10, 2008

Report

Report Number
2017865-2008-00945
Event Type
Death
Date Received
March 10, 2008
Date of Event
December 15, 2007
Manufacturer
ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION
Product Code
LWS
Removal / Correction Number
NA
Adverse Event
Yes
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
FL, US
Reporter Occupation
PHYSICIAN

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 CURRENT RF DR IMPLANTABLE CARDIOVERTER DEFIBRILLATOR LWS ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION 2207-36 NA

Patients

Seq Age Sex Outcome Treatment
1 * Death