FDA Adverse Event Injury Summary report: N

SPRINT QUATTRO SECURE S

MDR report key: 2791243 · Received October 15, 2012

Report

Report Number
2649622-2012-14815
Event Type
Injury
Date Received
October 15, 2012
Date of Event
August 19, 2012
Manufacturer
MEDTRONIC PUERTO RICO, INC.
Product Code
LWS
PMA / PMN Number
P920015/S039
Removal / Correction Number
Z-0474-2011
Adverse Event
Yes
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
MN, 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 THE PATIENT WENT TO THE EMERGENCY DEPARTMENT DUE TO INAPPROPRIATE SHOCKS CAUSED BY THE VENTRICULAR LEAD OVERSENSING VERY LARGE T-WAVES. THE LEAD REMAINS IN USE. NO PATIENT COMPLICATIONS WERE 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 44 YR Hospitalization| L| O (B)(4) IMPLANTABLE PACEMAKER/CARDIO/DEFIB| 5076 IMPLANTABLE PACING LEAD| 1156T STJ IMPLANTABLE PACING LEAD