FDA Adverse Event Injury Summary report: N

EXCELLENCE+

MDR report key: 1072513 · Received July 10, 2008

Report

Report Number
2649622-2008-03723
Event Type
Injury
Date Received
July 10, 2008
Date of Event
October 17, 2007
Manufacturer
MEDTRONIC PUERTO RICO, INC.
Product Code
DTB
Removal / Correction Number
NI
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
FL
Reporter Occupation
INVALID DATA

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 EXCELLENCE+ IMPLANTABLE PACING LEAD DTB MEDTRONIC PUERTO RICO, INC. IMD49B NA

Patients

Seq Age Sex Outcome Treatment
1 84 YR Required Intervention 8042 IMPLANTABLE PULSE GENERATOR| IMS49JB IMPLANTABLE PACING LEAD