FDA Adverse Event Death Summary report: N

NONE

MDR report key: 1071214 · Received June 27, 2008

Report

Report Number
2649622-2008-03267
Event Type
Death
Date Received
June 27, 2008
Date of Event
March 29, 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 NONE IMPLANTABLE PACING LEAD DTB MEDTRONIC PUERTO RICO, INC. 4058M NA

Patients

Seq Age Sex Outcome Treatment
1 88 YR Other 4024 IMPLANTABLE PACING LEAD| 7108 IMPLANTABLE PULSE GENERATOR