FDA Adverse Event Injury Summary report: N

RIATA ST OPTIM ACTIVE FIXATION

MDR report key: 1010634 · Received March 10, 2008

Report

Report Number
2017865-2008-01185
Event Type
Injury
Date Received
March 10, 2008
Date of Event
August 9, 2007
Manufacturer
ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION
Product Code
LWS
Removal / Correction Number
NA
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
MD, US
Reporter Occupation
PHYSICIAN

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 RIATA ST OPTIM ACTIVE FIXATION DEFIBRILLATION LEAD LWS ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION 7020/60 NA

Patients

Seq Age Sex Outcome Treatment
1 * Required Intervention