FDA Adverse Event Injury Summary report: N

EASYTRAK 2

MDR report key: 1873952 · Received October 19, 2010

Report

Report Number
2124215-2010-17776
Event Type
Injury
Date Received
October 19, 2010
Date of Event
September 2, 2010
Report Date
September 2, 2010
Manufacturer
CPI - DEL CARIBE
Product Code
OJX
PMA / PMN Number
P010012
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

AT THIS TIME, THIS LEAD HAS NOT BEEN RETURNED. IF ADDITIONAL INFORMATION IS RECEIVED, THIS REPORT WILL BE UPDATED.

Description of Event or Problem · 1

BOSTON SCIENTIFIC CRM RECEIVED INFORMATION THAT THIS LEFT VENTRICULAR (LV) LEAD WAS EXPLANTED DUE TO AN INFECTION.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 EASYTRAK 2 IMPLANTABLE LEAD OJX CPI - DEL CARIBE 4543

Patients

Seq Age Sex Outcome Treatment
1 79 YR Required Intervention H177| 4469| 0184| 4543