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News Opinion Editor's Corner

TCTMD’s Top 10 Most Popular Stories for July 2025

Caitlin E. Cox

July 31, 2025

News Opinion Editor's Corner

TCTMD’s Top 10 Most Popular Stories for June 2025

Michael O'Riordan

June 30, 2025

Presentation TCT 2024

TCT 474: Adverse Events and Failure Modes Related to Impella CP: Insights From the FDA MAUDE Database

Presenter: Kalyan Chitturi

October 28, 2024

Presentation TCT 2024

TCT 473: Adverse Events and Failure Modes Related to Impella RP/RP Flex: Insights From the FDA MAUDE Database

Presenter: Kalyan Chitturi

October 28, 2024

Presentation TCT 2023

TCT 435: Adverse Events with Intravascular Lithotripsy After Coronary Use: A Report from the FDA MAUDE Database

Presenter: Athanasios Rempakos

October 25, 2023

Presentation TCT 2022

TCT 173: Complications and Failure Modes of The Angiovac Thrombectomy System: Insight from MAUDE Database

Presenter: Rashid Alhusain

September 18, 2022

News Daily News

VASCADE Closure Device: FDA Database Tracks Common Complications, Deaths

Caitlin E. Cox

September 10, 2021

News Daily News

No Harm, No Help With Bioabsorbable-Polymer Stents: Registry

Michael O'Riordan

March 01, 2021

News Daily News

More Acute Stent Thrombosis With Synergy Stent in Bern PCI Registry

Michael O'Riordan

August 14, 2019

News Conference News CRT 2019

Adverse Events Reports for Guide Extension Catheter Should Spur Cautious Use

Yael L. Maxwell

March 05, 2019

Presentation CRT 2019

Adverse Events Associated with the Use of Guide Extension Catheters during Percutaneous Coronary Intervention: Reports From the Manufacturer and User Facility Device Experience (MAUDE) database

Presenter: Yuefeng Chen

March 05, 2019

News Daily News

FDA Warns of Class I Recall of Chariot Guiding Sheath Used in Peripheral Procedures

Shelley Wood

December 10, 2015

News Daily News

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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TCTMD’s Top 10 Most Popular Stories for July 2025

TCTMD’s Top 10 Most Popular Stories for June 2025

TCT 474: Adverse Events and Failure Modes Related to Impella CP: Insights From the FDA MAUDE Database

TCT 473: Adverse Events and Failure Modes Related to Impella RP/RP Flex: Insights From the FDA MAUDE Database

TCT 435: Adverse Events with Intravascular Lithotripsy After Coronary Use: A Report from the FDA MAUDE Database

TCT 173: Complications and Failure Modes of The Angiovac Thrombectomy System: Insight from MAUDE Database

VASCADE Closure Device: FDA Database Tracks Common Complications, Deaths

No Harm, No Help With Bioabsorbable-Polymer Stents: Registry

More Acute Stent Thrombosis With Synergy Stent in Bern PCI Registry

Adverse Events Reports for Guide Extension Catheter Should Spur Cautious Use

Adverse Events Associated with the Use of Guide Extension Catheters during Percutaneous Coronary Intervention: Reports From the Manufacturer and User Facility Device Experience (MAUDE) database

FDA Warns of Class I Recall of Chariot Guiding Sheath Used in Peripheral Procedures

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

FDA对在房颤患者中使用Lariat左心耳封堵装置发出警示

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

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