FDA Adverse Event Death Summary report: N

RESOLUTE ONYX RX

MDR report key: 8037827 · Received November 5, 2018

Report

Report Number
9612164-2018-03041
Event Type
Death
Date Received
November 5, 2018
Date of Event
September 15, 2018
Report Date
September 20, 2019
Manufacturer
MEDTRONIC IRELAND
Product Code
NIQ
PMA / PMN Number
P160043
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
MY
Reporter Occupation
PHYSICIAN

Narratives

Additional Manufacturer Narrative · 1

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

Additional Manufacturer Narrative · 1

CEC ASSESSED THAT THE MI WAS A NON EVENT. CEC ASSESSED THE DEATH AS CARDIAC DEATH AND ARC PROBABLE SUBACUTE STENT THROMBOSIS IN THE TARGET VESSEL LAD. IF INFORMATION IS PROVIDED IN THE FUTURE, A SUPPLEMENTAL REPORT WILL BE ISSUED.

Additional Manufacturer Narrative · 1

PATIENT HAD TWO ADDITIONAL RESOLUTE ONYX DES IMPLANTED IN THE 1ST DIAGONAL AND LAD. IF INFORMATION IS PROVIDED IN THE FUTURE, A SUPPLEMENTAL REPORT WILL BE ISSUED.

Additional Manufacturer Narrative · 1

ADDITIONAL INFORMATION: CEC COMMENTED THAT PATIENT ADMITTED WITH NSTEMI. NO CHANGE IN ADJUDICATION. IF INFORMATION IS PROVIDED IN THE FUTURE, A SUPPLEMENTAL REPORT WILL BE ISSUED.

Description of Event or Problem · 1

DURING THE INDEX PROCEDURE ONE RESOLUTE ONYX DES WAS IMPLANTED IN THE LAD. TWO DAYS POST INDEX PROCEDURE, THE PATIENT DIED. CAUSE OF DEATH IS ACUTE CORONARY SYNDROME TRO ISR. THE INVESTIGATOR ASSESSED THE EVENT AS NOT RELATED TO THE INDEX DEVICE OR ANTIPLATELET MEDICATION. SAFETY ASSESSED THE EVENT AS NOT RELATED TO THE DEVICE OR ANTIPLATELET MEDICATION.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
877757 RESOLUTE ONYX RX STENT, CORONARY, DRUG-ELUTING NIQ MEDTRONIC IRELAND 0009136654

Patients

Seq Age Sex Outcome Treatment
1 36 YR Death