FDA Adverse Event Injury Summary report: N

SPRINT

MDR report key: 1072794 · Received July 10, 2008

Report

Report Number
2649622-2008-03291
Event Type
Injury
Date Received
July 10, 2008
Date of Event
November 13, 2006
Manufacturer
MEDTRONIC PUERTO RICO, INC.
Product Code
LWS
Removal / Correction Number
NI
Adverse Event
Yes
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
WA
Reporter Occupation
INVALID DATA

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 SPRINT IMPLANTABLE TACHY LEAD LWS MEDTRONIC PUERTO RICO, INC. 6943 NA

Patients

Seq Age Sex Outcome Treatment
1 70 YR Required Intervention 7227CX IMPLANTABLE PACEMAKER/CARDIO/DEFIB