FDA Adverse Event Injury Summary report: N

WATCHMAN LAA CLOSURE DEVICE & DELIVERY SYSTEM

MDR report key: 18597700 · Received January 29, 2024

Report

Report Number
2124215-2024-02226
Event Type
Injury
Date Received
January 29, 2024
Date of Event
November 1, 2014
Report Date
January 29, 2024
Manufacturer
BOSTON SCIENTIFIC CORPORATION
Product Code
NGV
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
BE
Reporter Occupation
PHYSICIAN
Health Professional
Yes

Narratives

Additional Manufacturer Narrative · 0

B3: DATE OF EVENT - ESTIMATED AS 01NOV2014 AS THE DATE RANGE IS FROM NOVEMBER 2014 TO APRIL 2022. THIS LITERATURE IDENTIFIED PERIPROCEDURAL COMPLICATIONS RELATING TO WATCHMAN AND NON-BSC PRODUCTS INCLUDING DEATH. THE 2 DEATHS WERE IDENTIFIED AS DUPLICATES TO EXISTING COMPLAINTS. LITERATURE CITATION: AMINIAN A, LEDUC N, FREIXA X, SWAANS MJ, BEN YEDDER M, MAARSE M, SANCHIS L, CEPAS-GUILLEN P, CRUZ-GONZALEZ I, BLANCO-FERNANDEZ F, ESCHALIER R, BOERSMA LVA. LEFT ATRIAL APPENDAGE OCCLUSION UNDER MINIATURIZED TRANSESOPHAGEAL ECHOCARDIOGRAPHIC GUIDANCE AND CONSCIOUS SEDATION: MULTICENTER EUROPEAN EXPERIENCE. JACC CARDIOVASC INTERV. 2023 AUG 14;16(15):1889-1898. DOI: 10.1016/J.JCIN.2023.06.007. PMID: 37587597.

Description of Event or Problem · 0

IT WAS REPORTED VIA LITERATURE THAT CARDIAC TAMPONADE (MAJOR BLEEDING) AND TRANSIENT ISCHEMIC ATTACK (TIA) OCCURRED. LEFT ATRIAL APPENDAGE OCCLUSION (LAAO) PROCEDURES WERE PERFORMED WITH MINIATURIZED TRANSESOPHAGEAL ECHOCARDIOGRAPHY (TEE) PROBES FOR 546 PATIENTS BETWEEN (B)(6) 2014 AND (B)(6) 2022. OF THE IMPLANTED DEVICES FROM THE STUDY, 301 WERE ATTRIBUTED TO THE WATCHMAN PRODUCT. A TOTAL OF 16 PERIPROCEDURAL CLINICAL OUTCOMES OCCURRED IN 15 PATIENTS. THE PERIPROCEDURAL COMPLICATIONS INCLUDED CARDIAC TAMPONADE IN 9 PATIENTS, MAJOR BLEEDING EVENTS IN 4 PATIENTS, TRANSIENT ISCHEMIC ATTACK (TIA) IN 1 PATIENT, AND DEATH IN 2 PATIENTS. ONE PATIENT DEVELOPED SEVERE PROCEDURAL TAMPONADE DUE TO ATRIAL PERFORATION REQUIRING LAA SURGICAL REPAIR AND LIGATION AND ULTIMATELY DIED FROM POSTOPERATIVE CIRCULATORY SHOCK AND MULTIORGAN FAILURE. THE OTHER PATIENT DIED FROM TYPE 2 ACUTE CORONARY SYNDROME IN THE SETTING OF RECURRENT AND SEVERE GASTROINTESTINAL BLEEDING EVENTS.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
825746 WATCHMAN LAA CLOSURE DEVICE & DELIVERY SYSTEM SYSTEM, APPENDAGE CLOSURE, LEFT ATRIAL NGV BOSTON SCIENTIFIC CORPORATION

Patients

Seq Age Sex Outcome Treatment
1 Unknown Other