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FDA Warns of Air Embolism Risk With Watchman LAAO Access Systems

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FDA Warns of Air Embolism Risk With Watchman LAAO Access Systems

August 06, 2025

Class I Recall for Amplatzer LAAO's Steerable Delivery Sheath

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Class I Recall for Amplatzer LAAO's Steerable Delivery Sheath

July 26, 2023

Radiation Exposure ‘Extraordinarily’ High for Imagers in Structural Procedures

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Radiation Exposure ‘Extraordinarily’ High for Imagers in Structural Procedures

Yael L. Maxwell

July 11, 2022

FDA Investigating Possible Sex Differences in LAAO Outcomes

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FDA Investigating Possible Sex Differences in LAAO Outcomes

September 27, 2021

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La FDA Da la Voz de Alarma sobre el Uso del Dispositivo Lariat para el Cierre del AAI en Pacientes con FA

Yael L. Maxwell

July 17, 2015

News Daily News

FDA对在房颤患者中使用Lariat左心耳封堵装置发出警示

Yael L. Maxwell

July 17, 2015

News Daily News

FDA Sounds Alarm Bells Over Use of Lariat Device for LAA Closure in A-fib Patients

Yael L. Maxwell

July 17, 2015

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