FDA Adverse Event Injury Summary report: N

ST JUDE MEDICAL

MDR report key: 1031069 · Received April 9, 2008

Report

Report Number
1031069
Event Type
Injury
Date Received
April 9, 2008
Date of Event
March 26, 2008
Report Date
March 28, 2008
Manufacturer
ST. JUDE MEDICAL, CARDIAC RHYTHM MANAGEMENT DIV.
Product Code
LWS
Product Problem
Yes
Report Source
User Facility report
Reporter Location
MD, US
Reporter Occupation
NURSE

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 ST JUDE MEDICAL RIATA ST LEAD LWS ST. JUDE MEDICAL, CARDIAC RHYTHM MANAGEMENT DIV. 7002/60 *

Patients

Seq Age Sex Outcome Treatment
1 79 YR Hospitalization| L| R