FDA Adverse Event Death Summary report: N

ADAPTA DR

MDR report key: 3953551 · Received July 23, 2014

Report

Report Number
3004209178-2014-13438
Event Type
Death
Date Received
July 23, 2014
Date of Event
June 25, 2014
Report Date
February 20, 2015
Manufacturer
MEDTRONIC MED REL MEDTRONIC PUERTO RICO
Product Code
NVZ
PMA / PMN Number
P980035
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
MN, US
Reporter Occupation
OTHER

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. (B)(4).

Description of Event or Problem · 1

ADDITIONAL INFORMATION RECEIVED FROM THE HOSPITAL REPORTED THAT THE PATIENT BECAME UNRESPONSIVE AT HOME. AN AMBULANCE WAS CALLED AND THE PATIENT WAS FOUND TO BE IN ASYSTOLE. RESUSCITATION EFFORTS WERE INITIATED AND A PULSE AND RHYTHM RETURNED. UPON ARRIVAL TO THE EMERGENCY ROOM THE PATIENT WENT INTO PULSELESS ELECTRICAL ACTIVITY. RESUSCITATION EFFORTS WERECONTINUED AND WERE NOT SUCCESSFUL. ONE WEEK PRIOR TO DEATH AN ECHOCARDIOGRAM REPORT NOTED MODERATE PULMONARY STENOSIS AND PULMONARY REGURGITATION. THE PATIENT WAS TO HAVE A CARDIAC CATHETERIZATION BUT WAS TO WAIT TO ALLOW FURTHER RECOVERY FROM ATRIAL SEPTAL DEFECT REPAIR TWO MONTHS PRIOR AND RECENT VIRAL ILLNESSES.

Description of Event or Problem · 1

IT WAS REPORTED THE PATIENT IS DECEASED. A CALL RECEIVED FROM THE FUNERAL HOME INDICATED THE PATIENT'S REMOTE MONITOR WAS BROUGHT TO THEIR FACILITY IN ORDER TO SEND A FINAL DEVICE TRANSMISSION TO THE CLINIC. FURTHER REVIEW OF THE MANUFACTURER¿S DATABASE INDICATED THE PATIENT DIED APPROXIMATELY TWO MONTHS POST IMPLANT OF THE IMPLANTABLE PULSE GENERATOR (IPG) SYSTEM. ADDITIONAL INFORMATION OBTAINED REPORTED THE CAUSE OF DEATH AS: CARDIAC ARREST DUE TO ASYSTOLE COMPLICATED BY CONGENITAL HEART DISEASE, TETRALOGY OF FALLOT, VENTRICULAR SEPTAL DEFECT, SINUS BRADYCARDIA, PROLONGED QT INTERVAL, STATUS-POST SURGICAL REPAIR OF HEART ANOMALIES AND PACEMAKER. ADDITIONAL INFORMATION SURROUNDING THE CIRCUMSTANCES OF THE PATIENT DEATH HAVE BEEN REQUESTED AND NOT RECEIVED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
429886 ADAPTA DR PULSE GENERATOR, PERMANENT, IMPLANTABLE NVZ MEDTRONIC MED REL MEDTRONIC PUERTO RICO ADDR01

Patients

Seq Age Sex Outcome Treatment
1 00012 MO Death 4968-25 LEAD, 4968-25 LEAD