FDA Adverse Event Injury Summary report: N

SWEET TIP

MDR report key: 1863691 · Received October 11, 2010

Report

Report Number
2124215-2010-15844
Event Type
Injury
Date Received
October 11, 2010
Date of Event
August 2, 2010
Report Date
August 2, 2010
Manufacturer
HISTORICAL PUERTO RICO
Product Code
NVN
Product Problem
Yes
Report Source
Manufacturer report
Reporter Occupation
HEALTH PROFESSIONAL

Narratives

Additional Manufacturer Narrative · 1

IF ADDITIONAL INFORMATION BECOMES AVAILABLE, THIS EVENT WILL BE UPDATED AS NECESSARY.

Description of Event or Problem · 1

BOSTON SCIENTIFIC CRM RECEIVED INFORMATION THAT THIS PRODUCT WAS PART OF A SYSTEM EXPLANT DUE TO A PATIENT INFECTION. 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 TIP IMPLANTABLE LEAD NVN HISTORICAL PUERTO RICO 4269

Patients

Seq Age Sex Outcome Treatment
1 76 YR Required Intervention (B)(4)| 4261| 1230| 4269