FDA Adverse Event Injury Summary report: N

VICTORY XL SR

MDR report key: 1011144 · Received March 10, 2008

Report

Report Number
2017865-2008-00675
Event Type
Injury
Date Received
March 10, 2008
Date of Event
September 27, 2007
Manufacturer
ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION
Product Code
DXY
Removal / Correction Number
NA
Adverse Event
Yes
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
FR
Reporter Occupation
PHYSICIAN

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 VICTORY XL SR IMPLANTABLE PACEMAKER PULSE GENERATOR DXY ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION 5610 NA

Patients

Seq Age Sex Outcome Treatment
1 * Required Intervention