FDA Adverse Event Injury Summary report: N

SWEET PICOTIP

MDR report key: 1951442 · Received January 6, 2011

Report

Report Number
2124215-2010-22898
Event Type
Injury
Date Received
January 6, 2011
Date of Event
November 23, 2010
Report Date
November 23, 2010
Manufacturer
CPI - DEL CARIBE
Product Code
NVN
PMA / PMN Number
P960006
Product Problem
Yes
Report Source
Manufacturer report
Reporter Occupation
MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

Narratives

Additional Manufacturer Narrative · 1

AS NO FURTHER INFORMATION CONCERNING THIS REPORT IS EXPECTED, OUR INVESTIGATION IS COMPLETE. THIS INVESTIGATION WILL BE UPDATED SHOULD FURTHER INFORMATION BE PROVIDED.

Description of Event or Problem · 1

BOSTON SCIENTIFIC RECEIVED INFORMATION THAT THIS PRODUCT WAS PART OF A SYSTEM EXPLANT DUE TO A POCKET EROSION. THERE WAS NO REPORT OF ADVERSE PATIENT EFFECTS DUE TO THE EXPLANT PROCEDURE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 SWEET PICOTIP IMPLANTABLE LEAD NVN CPI - DEL CARIBE 4053

Patients

Seq Age Sex Outcome Treatment
1 60 YR Required Intervention 0144| T165| 4053| 1861| E110