FDA Adverse Event Injury Summary report: N

SWEET PICOTIP

MDR report key: 3240051 · Received July 22, 2013

Report

Report Number
2124215-2013-09406
Event Type
Injury
Date Received
July 22, 2013
Date of Event
May 16, 2013
Report Date
May 16, 2013
Manufacturer
CPI - DEL CARIBE
Product Code
NVN
PMA / PMN Number
P960006
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
CA
Reporter Occupation
PHYSICIAN

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 REVISION DUE TO INFECTION. THERE WERE NO ADDITIONAL ADVERSE EFFECTS REPORTED. ADDITIONAL INFORMATION RECEIVED INDICATES THAT THE PATIENT HAD ENDOCARDITIS. THE PRODUCT WAS EXPLANTED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
341124 SWEET PICOTIP IMPLANTABLE LEAD NVN CPI - DEL CARIBE 4054

Patients

Seq Age Sex Outcome Treatment
1 76 YR Hospitalization| L| R 497-15| 1861| 497-05| 4054| T165| 0154| 101-05| 101-01