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News Daily News

Class I Recall for 330,000 Radial Artery Catheterization Kits: FDA

Yael L. Maxwell

April 03, 2024

News Daily News

FDA: No Signs of Link Between GLP-1s and Suicidal Thoughts, Actions

Todd Neale

January 12, 2024

News Daily News

Class I Recall for 350,000 Medtronic Defibrillators: FDA

Michael O'Riordan

July 19, 2023

News Daily News

Generic Dabigatran Lots Pulled for Nitrosamine Impurity

Michael O'Riordan

March 28, 2023

News Daily News

Uptick in ‘Implausible’ Cancers Reported After ARB Recalls

L.A. McKeown

August 20, 2021

News Daily News

Papers Probe Temporal Link Between COVID-19 Vaccines and Myocarditis

Michael O'Riordan

June 17, 2021

News Daily News

FDA Advisors Recommend CVD Event Reduction Claim for Icosapent Ethyl

Michael O'Riordan

November 14, 2019

News Daily News

FDA: Class I Recall for CentriMag Circulatory Support System Motor

Caitlin E. Cox

November 07, 2019

News Daily News

FDA Tallies Cases of Fournier Gangrene in Patients Taking SGLT2 Inhibitors

Michael O'Riordan

May 08, 2019

News Daily News

FDA Alerts Doctors to Potential Late Risks With Paclitaxel-Coated Balloons and Stents in PAD

Michael O'Riordan

January 17, 2019

News Daily News

FDA Warns of Rising Endoleak Rates After Endovascular Aneurysm Repair

L.A. McKeown

October 02, 2017

News Features

Absorb in Europe: When, How, and by Whom the Beleaguered BVS Is Being Used After Restrictions

Michael O'Riordan

May 08, 2017

News Daily News

Absorb BVS Use Restricted in Europe

Michael O'Riordan

April 06, 2017

News Conference News ACC 2017

FDA Warns of Risk of Major Adverse Cardiac Events With Absorb BVS

Michael O'Riordan

March 18, 2017

News Daily News

FDA Announces Recall of Bard’s Halo One Peripheral Vascular Guiding Sheath

L.A. McKeown

January 31, 2017

News Daily News

Vascular Solutions Recalls Twin-Pass Dual-Access Catheters

Michael O'Riordan

October 06, 2016

News Daily News

Cook Medical Issues Recall for Beacon Tip Catheters

Shelley Wood

May 04, 2016

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Class I Recall for 330,000 Radial Artery Catheterization Kits: FDA

FDA: No Signs of Link Between GLP-1s and Suicidal Thoughts, Actions

Class I Recall for 350,000 Medtronic Defibrillators: FDA

Generic Dabigatran Lots Pulled for Nitrosamine Impurity

Uptick in ‘Implausible’ Cancers Reported After ARB Recalls

Papers Probe Temporal Link Between COVID-19 Vaccines and Myocarditis

FDA Advisors Recommend CVD Event Reduction Claim for Icosapent Ethyl

FDA: Class I Recall for CentriMag Circulatory Support System Motor

FDA Tallies Cases of Fournier Gangrene in Patients Taking SGLT2 Inhibitors

FDA Alerts Doctors to Potential Late Risks With Paclitaxel-Coated Balloons and Stents in PAD

FDA Warns of Rising Endoleak Rates After Endovascular Aneurysm Repair

Absorb in Europe: When, How, and by Whom the Beleaguered BVS Is Being Used After Restrictions

Absorb BVS Use Restricted in Europe

FDA Warns of Risk of Major Adverse Cardiac Events With Absorb BVS

FDA Announces Recall of Bard’s Halo One Peripheral Vascular Guiding Sheath

Vascular Solutions Recalls Twin-Pass Dual-Access Catheters

Cook Medical Issues Recall for Beacon Tip Catheters

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