FDA Adverse Event Injury Summary report: N

SELUTE PICOTIP

MDR report key: 3211324 · Received July 8, 2013

Report

Report Number
2124215-2013-08425
Event Type
Injury
Date Received
July 8, 2013
Date of Event
May 7, 2013
Report Date
May 3, 2013
Manufacturer
CPI - DEL CARIBE
Product Code
NVN
Adverse Event
Yes
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
FL
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 RIGHT VENTRICULAR (RV) LEAD EXHIBITED LOSS OF CAPTURE. THE LEAD WAS SURGICALLY ABANDONED AND A NEW RV LEAD IMPLANTED WITHOUT ISSUE. THERE WERE NO ADDITIONAL ADVERSE PATIENT EFFECTS REPORTED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
311730 SELUTE PICOTIP IMPLANTABLE LEAD NVN CPI - DEL CARIBE 4035

Patients

Seq Age Sex Outcome Treatment
1 61 YR Hospitalization| L| R 1290| 4136| K063| 4035| 4087