FDA Adverse Event Injury Summary report: N

INSYNC SENTRY

MDR report key: 1072379 · Received July 10, 2008

Report

Report Number
6000144-2008-00147
Event Type
Injury
Date Received
July 10, 2008
Date of Event
April 3, 2007
Manufacturer
MEDTRONIC MED REL, INC.
Product Code
NIK
Removal / Correction Number
NI
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
IA
Reporter Occupation
INVALID DATA

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 INSYNC SENTRY IMPLANTABLE PACEMAKER/CARDIO/DEFIB NIK MEDTRONIC MED REL, INC. 7299 NA

Patients

Seq Age Sex Outcome Treatment
1 84 YR Other 5076 IMPLANTABLE PACING LEAD| 6947 IMPLANTABLE TACHY LEAD| 2187 IMPLANTABLE PACING LEAD