FDA Adverse Event Injury Summary report: N

EASYTRAK 2

MDR report key: 2041197 · Received April 6, 2011

Report

Report Number
2124215-2011-00985
Event Type
Injury
Date Received
April 6, 2011
Date of Event
January 11, 2011
Report Date
January 11, 2011
Manufacturer
CPI - DEL CARIBE
Product Code
OJX
PMA / PMN Number
P010012
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
TX
Reporter Occupation
MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

Narratives

Additional Manufacturer Narrative · 1

NO OTHER ADVERSE EVENTS HAVE BEEN REPORTED. THIS ISSUE WILL BE RE-EVALUATED IF ADDITIONAL INFORMATION IS RECEIVED.

Description of Event or Problem · 1

BOSTON SCIENTIFIC RECEIVED INFORMATION THAT THIS SYSTEM WAS EXPLANTED SECONDARY TO INFECTION.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 EASYTRAK 2 IMPLANTABLE LEAD OJX CPI - DEL CARIBE 4518

Patients

Seq Age Sex Outcome Treatment
1 67 YR 4518| N118| 4137| H219| 4470| 0185