FDA Adverse Event Injury Summary report: N

MEDTRONIC, INC.

MDR report key: 807378 · Received January 3, 2007

Report

Report Number
807378
Event Type
Injury
Date Received
January 3, 2007
Date of Event
December 11, 2006
Report Date
December 29, 2006
Manufacturer
MEDTRONIC, INC.
Product Code
DXY
Report Source
User Facility report
Reporter Location
HI, US
Reporter Occupation
RISK MANAGER

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 MEDTRONIC, INC. GENERATOR DXY MEDTRONIC, INC. 7960 NA
2 MEDTRONIC, INC. LEAD DTB MEDTRONIC, INC. 5034-52 NA

Patients

Seq Age Sex Outcome Treatment
1 86 YR Required Intervention