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  • (-) 2019 (45)
Displaying 21 - 40 of 45
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FDA Class I Recall for PTA Catheters Due to Unexpected Balloon Bursting
News Daily News

FDA Class I Recall for PTA Catheters Due to Unexpected Balloon Bursting

Yael L. Maxwell
Yael L. Maxwell
June 18, 2019
Early Bird Bleed Monitoring System Shows Promise in Endovascular Procedures
News Conference News SCAI 2019

Early Bird Bleed Monitoring System Shows Promise in Endovascular Procedures

Yael L. Maxwell
Yael L. Maxwell
May 31, 2019
TCTMD’s Top 10 Most Popular Stories for May 2019
News Opinion Editor's Corner

TCTMD’s Top 10 Most Popular Stories for May 2019

Caitlin E. Cox
Caitlin E. Cox
May 31, 2019
Terumo’s Solopath Transfemoral System and Recollapsible Balloon Access System Recalled for Dislodging Issues
News Daily News

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

L.A. McKeown
L.A. McKeown
May 30, 2019
FDA Provides Update on Poorer Survival With Impella RP in Postmarket Setting
News Daily News

FDA Provides Update on Poorer Survival With Impella RP in Postmarket Setting

Todd Neale
Todd Neale
May 21, 2019
FDA Tallies Cases of Fournier Gangrene in Patients Taking SGLT2 Inhibitors
News Daily News

FDA Tallies Cases of Fournier Gangrene in Patients Taking SGLT2 Inhibitors

Michael O'Riordan
Michael O'Riordan
May 08, 2019
FDA Warns of Premature Battery Depletion With Certain Medtronic Pacemakers
News Daily News

FDA Warns of Premature Battery Depletion With Certain Medtronic Pacemakers

Michael O'Riordan
Michael O'Riordan
May 07, 2019
TCTMD’s Top 10 Most Popular Stories for April 2019
News Daily News

TCTMD’s Top 10 Most Popular Stories for April 2019

Shelley Wood
Shelley Wood
May 01, 2019
Two Pediatric Cardiac Catheters Recalled for Defective Balloons
News Daily News

Two Pediatric Cardiac Catheters Recalled for Defective Balloons

L.A. McKeown
L.A. McKeown
April 26, 2019
FDA Warns Against Off-label Use of Wingspan Stent System
News Daily News

FDA Warns Against Off-label Use of Wingspan Stent System

Todd Neale
Todd Neale
April 25, 2019
FDA Warns of Cybersecurity Vulnerabilities With Some Medtronic Implanted Devices
News Daily News

FDA Warns of Cybersecurity Vulnerabilities With Some Medtronic Implanted Devices

Michael O'Riordan
Michael O'Riordan
March 22, 2019
FDA: Some Tainted Losartan Must Remain on US Market to Maintain Adequate Access for Patients
News Daily News

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

L.A. McKeown
L.A. McKeown
March 21, 2019
FDA Analysis Points to Higher Death Risk With Paclitaxel-Based Devices for PAD
News Daily News

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

L.A. McKeown
L.A. McKeown
March 15, 2019
FDA Provides Update on Tainted ARB Investigation, With New Impurity Found
News Daily News

FDA Provides Update on Tainted ARB Investigation, With New Impurity Found

Todd Neale
Todd Neale
March 04, 2019
New ALERTS Data Support Use of Implantable Cardiac Monitor in High-Risk ACS Patients—With Caveats
News Conference News CRT 2019

New ALERTS Data Support Use of Implantable Cardiac Monitor in High-Risk ACS Patients—With Caveats

Yael L. Maxwell
Yael L. Maxwell
March 03, 2019
TCTMD’s Top 10 Most Popular Stories for February 2019
News Daily News

TCTMD’s Top 10 Most Popular Stories for February 2019

Shelley Wood
Shelley Wood
March 01, 2019
Some Stryker Defibrillators Under Recall for ‘Freezing’ Issue
News Daily News

Some Stryker Defibrillators Under Recall for ‘Freezing’ Issue

Todd Neale
Todd Neale
February 27, 2019
FDA Adds Boxed Warning About CV Risks to Gout Drug Febuxostat
News Daily News

FDA Adds Boxed Warning About CV Risks to Gout Drug Febuxostat

Shelley Wood
Shelley Wood
February 22, 2019
Mortality Data ‘Inadvertently Omitted’ From IN.PACT Analysis of Paclitaxel-Coated Balloons
News Daily News

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

L.A. McKeown
L.A. McKeown
February 19, 2019
Class I Recall for Certain Medtronic Pacemakers Due to Possible Circuit Error
News Daily News

Class I Recall for Certain Medtronic Pacemakers Due to Possible Circuit Error

Todd Neale
Todd Neale
February 15, 2019

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