FDA Adverse Event Injury Summary report: N

SWEET PICOTIP

MDR report key: 1946162 · Received January 4, 2011

Report

Report Number
2124215-2010-21032
Event Type
Injury
Date Received
January 4, 2011
Date of Event
October 15, 2010
Report Date
October 15, 2010
Manufacturer
CPI - DEL CARIBE
Product Code
NVN
PMA / PMN Number
P960006
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
GA
Reporter Occupation
MEDICAL EQUIPMENT COMPANY TECHNICIAN/REPRESENTATIVE

Narratives

Additional Manufacturer Narrative · 1

THERE WERE NO ADDITIONAL ADVERSE EVENTS REPORTED.

Description of Event or Problem · 1

BOSTON SCIENTIFIC RECEIVED INFORMATION FROM AN OUT-OF-SERVICE FORM THAT THIS DEVICE HAD ERODED THROUGH THE SKIN WHICH LEAD TO AN INFECTION OF THE ENTIRE IMPLANTED SYSTEM. THE DEVICE AND LEADS WERE SUCCESSFULLY EXTRACTED AND THE PATIENT WAS PLACE ON ANTIBIOTIC THERAPY. THE PATIENT WILL BE SCHEDULED FOR A SYSTEM IMPLANT AT A LATER DATE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 SWEET PICOTIP IMPLANTABLE LEAD NVN CPI - DEL CARIBE 4054

Patients

Seq Age Sex Outcome Treatment
1 89 YR Hospitalization| L| R 4054| A155| 1831| E110| 0144