FDA Adverse Event Injury Summary report: N

RIATA 1580-65

MDR report key: 4475875 · Received January 27, 2015

Report

Report Number
MW5040516
Event Type
Injury
Date Received
January 27, 2015
Date of Event
January 21, 2015
Report Date
January 27, 2015
Manufacturer
ST. JUDE
Product Code
LWS
Product Problem
Yes
Report Source
Voluntary report
Reporter Location
NY, US
Reporter Occupation
NURSE

Narratives

Description of Event or Problem · 1

A (B)(6) WM WITH NICM, HISTORY OF RECURRENT VT, S/P MDT ICD, NOW NOTED TO HAVE DYSFUNCTIONAL LV LEAD. PT ALSO NOTED TO HAVE STJ RIATA LEAD, ON ADVISORY, AND DEVICE NEARING ERI. HERE TODAY FOR RV LEAD REVISION AND ICD GENERATOR CHANGE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
63173 RIATA 1580-65 RIATA 1580-65 LWS ST. JUDE 1580-65

Patients

Seq Age Sex Outcome Treatment
1 52 YR Life Threatening| R