FDA Adverse Event Injury Summary report: N

SWEET TIP

MDR report key: 2780606 · Received October 10, 2012

Report

Report Number
2124215-2012-13436
Event Type
Injury
Date Received
October 10, 2012
Date of Event
September 13, 2012
Report Date
September 13, 2012
Manufacturer
CPI - DEL CARIBE
Product Code
NVN
PMA / PMN Number
K893957
Adverse Event
Yes
Product Problem
Yes
Report Source
Manufacturer report
Reporter Occupation
PHYSICIAN

Narratives

Additional Manufacturer Narrative · 1

THE SYSTEM WAS SUCCESSFULLY REPLACED. 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 REVISION DUE TO INFECTION. THERE WERE NO ADDITIONAL ADVERSE EFFECTS REPORTED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 SWEET TIP IMPLANTABLE LEAD NVN CPI - DEL CARIBE 4269

Patients

Seq Age Sex Outcome Treatment
1 69 YR Hospitalization| L| R 1821| 0015| 4269| 0095| T177| 0125| 1810