FDA Adverse Event Death Summary report: N

AMPLATZER SEPTAL OCCLUDER

MDR report key: 14467942 · Received May 23, 2022

Report

Report Number
2135147-2022-00307
Event Type
Death
Date Received
May 23, 2022
Report Date
June 18, 2022
Manufacturer
ABBOTT MEDICAL
Product Code
MLV
PMA / PMN Number
P000039
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
JA
Reporter Occupation
PHYSICIAN
Health Professional
Yes

Narratives

Additional Manufacturer Narrative · 0

INVESTIGATION IS NOT YET COMPLETE. A FOLLOW-UP REPORT WILL BE SUBMITTED WITH ALL ADDITIONAL RELEVANT INFORMATION. RELATED MANUFACTURER REFERENCE NUMBER: (B)(4).

Additional Manufacturer Narrative · 0

AS REPORTED IN A RESEARCH ARTICLE, (B)(4) UNDERWENT PERCUTANEOUS ASD CLOSURES BETWEEN (B)(6) 2014 AND (B)(6) 2020; THE DEVICES ASSOCIATED WITH THIS STUDY WERE AMPLATZER SEPTAL OCCLUDER (ASO) AND FIGULLA FLEX II SEPTAL OCCLUDER (FSO). THERE WERE NO DIFFERENCES IN THE CLINICAL PERFORMANCE OF DEATH BETWEEN THE TWO GROUPS. A MORE COMPREHENSIVE ASSESSMENT COULD NOT BE PERFORMED AS THE EVENT WAS NON-CONTEMPORANEOUSLY REPORTED THROUGH A LITERATURE REVIEW, AND NO DEVICE OR ADDITIONAL PATIENT INFORMATION WAS RECEIVED FOR ANALYSIS. BASED ON THE INFORMATION RECEIVED, THE CAUSE OF THE REPORTED INCIDENT COULD NOT BE CONCLUSIVELY DETERMINED.

Description of Event or Problem · 0

THE ARTICLE, "COMPARISON OF ANATOMICAL FEATURES AND POSTOPERATIVE CLINICAL RESULTS OF ASD BETWEEN TWO TYPES OF ASD CLOSURE DEVICES", WAS REVIEWED. THIS RESEARCH ARTICLE IS A RETROSPECTIVE SINGLE CENTER EXPERIENCE TO ANALYZE THE POSTOPERATIVE CLINICAL RESULTS BETWEEN BOTH DEVICES AND THE ANATOMICAL FEATURES OF EACH ATRIAL SEPTAL DEFECT IN THE HOSPITAL. DEVICES INVOLVED INCLUDED AMPLATZER SEPTAL OCCLUDER (ASO) AND FIGULLA FLEX II SEPTAL OCCLUDER (FSO). THE ARTICLE CONCLUDED THAT ASOS WERE PLACED IN POSTERIOR RIM DEFECT CASES AND FSOS IN AORTIC-SUPERIOR RIM DEFECT, SEPTAL M MALALIGNMENT, AND EXTENSIVE RIM DEFECT CASES, BUT THERE WERE NO DIFFERENCES IN PATIENT CHARACTERISTICS OR TREATMENT EFFICACY AND SAFETY OUTCOMES BETWEEN THE TWO DEVICES. THE AUTHOR OF THIS ARTICLE IS KOTARO MIURA, MD, DEPARTMENT OF CARDIOLOGY, KEIO UNIVERSITY HOSPITAL, 35 SHINANOMACHI, SHINJUKU-KU, TOKYO 160-8582.

Description of Event or Problem · 0

N/A.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1522097 AMPLATZER SEPTAL OCCLUDER TRANSCATHETER SEPTAL OCCLUDER MLV ABBOTT MEDICAL

Patients

Seq Age Sex Outcome Treatment
1 53 YR Unknown Death