FDA Adverse Event Death Summary report: N

ENTRUST

MDR report key: 2993567 · Received March 7, 2013

Report

Report Number
3004209178-2013-03468
Event Type
Death
Date Received
March 7, 2013
Date of Event
February 28, 2012
Report Date
May 25, 2021
Manufacturer
MEDTRONIC MED REL MEDTRONIC PUERTO RICO
Product Code
LWS
PMA / PMN Number
P980016
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
WI, US
Reporter Occupation
PHYSICIAN

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. ADDITIONAL INFORMATION WAS OBTAINED FROM THE PHYSICIAN'S OFFICE, AND PER THE HOSPITAL NOTE, THE PATIENT WAS ADMITTED TO HOSPITAL FOR SEPTIC SHOCK DUE TO STREPTOCOCCUS (THE STRAIN WAS NOT PROVIDED). ALSO, VEGETATION WAS NOTED ON THE DEFIBRILLATION LEAD. THE PATIENT'S COURSE PROGRESSED TO RENAL INSUFFICIENCY, HEMODYNAMIC INSTABILITY AND DEATH. THE SOURCE OF THE SEPSIS AND THE CAUSE OF DEATH WERE REQUESTED AND NOT RECEIVED. FOLLOW-UP IS IN PROGRESS. THE DECISION TO REPORT WAS DETERMINED BASED ON INFORMATION THAT WAS AVAILABLE AT THE TIME OF DECISION. SHOULD ADDITIONAL INFORMATION BECOME KNOWN THROUGH FOLLOW-UP, IT WILL BE ADDED TO THE EVENT AND PROCESSED ACCORDINGLY. THE PRODUCT WAS RECEIVED BUT WILL NOT BE ANALYZED DUE TO A LEGAL HOLD. DEVICES: 5076 IMPLANTABLE PACING LEAD, (B)(6) 2006.

Additional Manufacturer Narrative · 1

IF INFORMATION IS PROVIDED IN THE FUTURE, A SUPPLEMENTAL REPORT WILL BE ISSUED.

Description of Event or Problem · 1

IT WAS REPORTED THE PATIENT IS DECEASED AND DIED APPROXIMATELY FIVE AND ONE-HALF YEARS POST THE IMPLANT OF THE PATIENT'S DUAL CHAMBER IMPLANTABLE CARDIOVERTER DEFIBRILLATOR (ICD) SYSTEM. NO FURTHER INFORMATION WAS PROVIDED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
97814 ENTRUST IMPLANTABLE CARDIOVERTER DEFIBRILLATOR (NON-CRT) LWS MEDTRONIC MED REL MEDTRONIC PUERTO RICO D154ATG

Patients

Seq Age Sex Outcome Treatment
1 00073 YR Death (B)(4) IMPLANTABLE TACHY LEAD| (B)(4) IMPLANTABLE TACHY LEAD