FDA Adverse Event Injury Summary report: N

SPRINT QUATTRO SECURE S

MDR report key: 2813191 · Received October 31, 2012

Report

Report Number
2649622-2012-16507
Event Type
Injury
Date Received
October 31, 2012
Date of Event
August 3, 2012
Manufacturer
MEDTRONIC PUERTO RICO, INC.
Product Code
LWS
PMA / PMN Number
P920015/S039
Adverse Event
Yes
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
MI, US
Reporter Occupation
HEALTH PROFESSIONAL

Narratives

Additional Manufacturer Narrative · 1

THE INFORMATION SUBMITTED REFLECTS ALL RELEVANT DATA RECEIVED. IF ADDITIONAL RELEVANT INFORMATION IS RECEIVED, A SUPPLEMENTAL REPORT WILL BE SUBMITTED.

Description of Event or Problem · 1

IT WAS REPORTED THAT THE PATIENT RECEIVED A SHOCK DUE TO T WAVE OVERSENSING ON THE RIGHT VENTRICULAR LEAD. IT WAS ALSO REPORTED THAT R WAVES HAVE BEEN CHRONICALLY LOW. INTERMITTENT OVERSENSING WAS OCCURRING REAL TIME. REPROGRAMMING TO TIP-COIL RESOLVED THE T WAVE OVERSENSING, AND R WAVES WERE ALSO IMPROVED. THE LEAD REMAINS IN USE. NO FURTHER PATIENT COMPLICATIONS HAVE BEEN REPORTED AS A RESULT OF THIS EVENT.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 SPRINT QUATTRO SECURE S IMPLANTABLE TACHY LEAD LWS MEDTRONIC PUERTO RICO, INC. 6935

Patients

Seq Age Sex Outcome Treatment
1 43 YR Life Threatening| R 4076 IMPLANTABLE PACING LEAD| (B)(4) IMPLANTABLE PACEMAKER/CARDIO/DEFIB