AMPLATZER AMULET
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
CORRECTION REPORT TO ADD EXEMPTION # GEN2201026.
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.
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 |