FDA Adverse Event Death Summary report: Y

AMPLATZER AMULET

MDR report key: 18017445 · Received October 27, 2023

Report

Report Number
2135147-2023-04729
Event Type
Death
Date Received
October 27, 2023
Date of Event
November 9, 2022
Report Date
September 23, 2024
Manufacturer
ABBOTT MEDICAL
Product Code
NGV
PMA / PMN Number
P200049
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
US
Reporter Occupation
PHYSICIAN
Health Professional
Yes

Narratives

Additional Manufacturer Narrative · 0

CORRECTION REPORT TO ADD EXEMPTION # GEN2201026.

Additional Manufacturer Narrative · 0

AMULET LAAO REGISTRY REPORTS 4 EVENTS OF SUDDEN CARDIAC DEATH. A MORE COMPREHENSIVE ASSESSMENT COULD NOT BE PERFORMED AS NO ADDITIONAL INFORMATION WAS RECEIVED FOR ANALYSIS. BASED ON THE INFORMATION RECEIVED, THE CAUSE OF THE REPORTED INCIDENT COULD NOT BE CONCLUSIVELY DETERMINED. THERE IS NO INDICATION OF A PRODUCT QUALITY ISSUE WITH REGARDS TO MANUFACTURE, DESIGN, OR LABELING. B2: DATE OF DEATH: THE EARLIEST DATE OF DEATH WAS USED. D6A: IMPLANT DATE: THE EARLIEST IMPLANT DATE WAS USED.

Description of Event or Problem · 0

IT WAS REPORTED THROUGH LEFT ATRIAL APPENDAGE OCCLUDER (LAAO) REGISTRY DATA THAT AMPLATZER AMULET DEVICES MAY BE RELATED TO 4 SUDDEN CARDIAC DEATH ADVERSE EVENTS WHICH ARE CONSIDERED A DEATH. THE RELATIONSHIP OF THE DEATHS TO THE AMPLATZER AMULET DEVICES COULD NOT BE DETERMINED BASED ON THE LIMITED DATA RECEIVED FROM THE REGISTRY. LEFT ATRIAL APPENDAGE OCCLUDER (LAAO) REGISTRY DATA IS REPORTED AS A SUMMARY PER SUMMARY REPORTING EXEMPTION APPROVAL NUMBER: GEN2201026. THE DATA RECEIVED INDICATED THAT THE PROCEDURE DATE RANGE WAS BETWEEN 09 NOVEMBER 2022 ¿ 11 MAY 2023. PATIENTS¿ MEAN AGE IS 85 YEARS, RANGING FROM 76 - 89 YEARS. 100% OF THE PATIENTS WERE MALE, 0% OF THE PATIENTS WERE FEMALE.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1023415 AMPLATZER AMULET CARDIAC PLUG NGV ABBOTT MEDICAL

Patients

Seq Age Sex Outcome Treatment
1 79 YR Unknown Death