FDA Adverse Event Injury Summary report: N

MARQUIS DR

MDR report key: 1013488 · Received March 10, 2008

Report

Report Number
6000094-2008-00074
Event Type
Injury
Date Received
March 10, 2008
Date of Event
June 18, 2007
Manufacturer
MEDTRONIC S.A.
Product Code
LWS
Removal / Correction Number
NI
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
TX
Reporter Occupation
INVALID DATA

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 MARQUIS DR IMPLANTABLE PACEMAKER/CARDIO/DEFIB LWS MEDTRONIC S.A. 7274 NA

Patients

Seq Age Sex Outcome Treatment
1 67 YR Other 4193 IMPLANTABLE PACING LEAD| 4068 IMPLANTABLE PACING LEAD| 6943 IMPLANTABLE TACHY LEAD