FDA Adverse Event Injury Summary report: N

MARQUIS DR

MDR report key: 1072108 · Received July 10, 2008

Report

Report Number
2647346-2008-00293
Event Type
Injury
Date Received
July 10, 2008
Date of Event
November 14, 2007
Manufacturer
MEDTRONIC MED REL, INC.
Product Code
LWS
Removal / Correction Number
NI
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
OH
Reporter Occupation
INVALID DATA

Devices

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

Patients

Seq Age Sex Outcome Treatment
1 84 YR Other 5076 IMPLANTABLE PACING LEAD| 6947 IMPLANTABLE TACHY LEAD