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News Daily News

Cardiology Societies Unite to Condemn Racism and Health Inequality

L.A. McKeown

June 01, 2020

News Daily News

FDA: Class I Recall for Vascular Solutions’ Dual Lumen Catheters

L.A. McKeown

May 01, 2020

News Daily News

FDA Class I Recall for Boston Scientific’s IMAGER II Angiographic Catheters

L.A. McKeown

April 07, 2020

News Daily News

FDA: Class I Recall for Cook Medical’s CrossCath Support Catheters

L.A. McKeown

December 17, 2019

News Daily News

FDA: New Concerns Surface With Endologix Grafts for AAA

L.A. McKeown

October 28, 2019

News Daily News

Terumo’s Solopath Transfemoral System and Recollapsible Balloon Access System Recalled for Dislodging Issues

L.A. McKeown

May 30, 2019

News Daily News

Two Pediatric Cardiac Catheters Recalled for Defective Balloons

L.A. McKeown

April 26, 2019

News Daily News

FDA: Some Tainted Losartan Must Remain on US Market to Maintain Adequate Access for Patients

L.A. McKeown

March 21, 2019

News Daily News

FDA Analysis Points to Higher Death Risk With Paclitaxel-Based Devices for PAD

L.A. McKeown

March 15, 2019

News Daily News

Mortality Data ‘Inadvertently Omitted’ From IN.PACT Analysis of Paclitaxel-Coated Balloons

L.A. McKeown

February 19, 2019

News Daily News

FDA Warns of Stroke and Arterial Dissection Risk With MS Drug

L.A. McKeown

November 29, 2018

News Daily News

FDA: All AFX Endovascular AAA Systems Now Under Class I Recall

L.A. McKeown

October 16, 2018

News Daily News

FDA Identifies Culprit in Endovascular Graft Type III Endoleaks

L.A. McKeown

June 19, 2018

News Daily News

FDA’s ‘Medical Device Safety Action Plan’ Focuses on Product Life Cycles and Preventing Cyberattacks

L.A. McKeown

April 20, 2018

News Daily News

Recall: Clopidogrel Tablets Mislabeled, May Contain Statin

L.A. McKeown

January 11, 2018

News Daily News

FDA Warns of Rising Endoleak Rates After Endovascular Aneurysm Repair

L.A. McKeown

October 02, 2017

News Daily News

IABPs Recalled Due to False Blood Detection Alarms and Ingress of Fluid

L.A. McKeown

September 06, 2017

News Daily News

FDA: Class I Recall for Venture Catheters

L.A. McKeown

June 21, 2017

News Daily News

FDA: Class I Recall for Over 47,000 HeartStart MRx Monitor/Defibrillator Units

L.A. McKeown

March 24, 2017

News Daily News

Abbott to Issue Urgent Recall of Certain Lots of Vascular Closure System

L.A. McKeown

February 10, 2017

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Cardiology Societies Unite to Condemn Racism and Health Inequality

FDA: Class I Recall for Vascular Solutions’ Dual Lumen Catheters

FDA Class I Recall for Boston Scientific’s IMAGER II Angiographic Catheters

FDA: Class I Recall for Cook Medical’s CrossCath Support Catheters

FDA: New Concerns Surface With Endologix Grafts for AAA

Terumo’s Solopath Transfemoral System and Recollapsible Balloon Access System Recalled for Dislodging Issues

Two Pediatric Cardiac Catheters Recalled for Defective Balloons

FDA: Some Tainted Losartan Must Remain on US Market to Maintain Adequate Access for Patients

FDA Analysis Points to Higher Death Risk With Paclitaxel-Based Devices for PAD

Mortality Data ‘Inadvertently Omitted’ From IN.PACT Analysis of Paclitaxel-Coated Balloons

FDA Warns of Stroke and Arterial Dissection Risk With MS Drug

FDA: All AFX Endovascular AAA Systems Now Under Class I Recall

FDA Identifies Culprit in Endovascular Graft Type III Endoleaks

FDA’s ‘Medical Device Safety Action Plan’ Focuses on Product Life Cycles and Preventing Cyberattacks

Recall: Clopidogrel Tablets Mislabeled, May Contain Statin

FDA Warns of Rising Endoleak Rates After Endovascular Aneurysm Repair

IABPs Recalled Due to False Blood Detection Alarms and Ingress of Fluid

FDA: Class I Recall for Venture Catheters

FDA: Class I Recall for Over 47,000 HeartStart MRx Monitor/Defibrillator Units

Abbott to Issue Urgent Recall of Certain Lots of Vascular Closure System

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