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Displaying 1 - 20 of 22
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Eye Condition a ‘Very Rare’ Side Effect of Semaglutide, EMA Says
News Daily News

Eye Condition a ‘Very Rare’ Side Effect of Semaglutide, EMA Says

Todd Neale
Todd Neale
June 06, 2025
Evoque and Patisiran: A Tale of Two Regulatory Journeys
News Opinion Off Script

Evoque and Patisiran: A Tale of Two Regulatory Journeys

Sanjay Kaul, MD
Sanjay Kaul, MD
March 29, 2024
FDA: Class I Recall for Left-Sided Impella Pumps Due to TAVI Interaction
News Daily News

FDA: Class I Recall for Left-Sided Impella Pumps Due to TAVI Interaction

Caitlin E. Cox
Caitlin E. Cox
July 27, 2023
Abiomed Recalls Certain Impella 5.5 Devices Due to Risk of Purge-Fluid Leaks
News Daily News

Abiomed Recalls Certain Impella 5.5 Devices Due to Risk of Purge-Fluid Leaks

Caitlin E. Cox
Caitlin E. Cox
June 05, 2023
Impella RP Mortality Rate No Longer a Concern, FDA Says
News Daily News

Impella RP Mortality Rate No Longer a Concern, FDA Says

Caitlin E. Cox
Caitlin E. Cox
December 05, 2022
Uptick in ‘Implausible’ Cancers Reported After ARB Recalls
News Daily News

Uptick in ‘Implausible’ Cancers Reported After ARB Recalls

L.A. McKeown
L.A. McKeown
August 20, 2021
Papers Probe Temporal Link Between COVID-19 Vaccines and Myocarditis
News Daily News

Papers Probe Temporal Link Between COVID-19 Vaccines and Myocarditis

Michael O'Riordan
Michael O'Riordan
June 17, 2021
Medtronic Recalls Valiant Navion TEVAR Stent Grafts
News Daily News

Medtronic Recalls Valiant Navion TEVAR Stent Grafts

Shelley Wood
Shelley Wood
February 17, 2021
Burst Balloons With Sapien 3 Ultra Prompt ‘Urgent Field Safety Notice’ and Canadian Recall
News Daily News

Burst Balloons With Sapien 3 Ultra Prompt ‘Urgent Field Safety Notice’ and Canadian Recall

Shelley Wood
Shelley Wood
July 22, 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 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
FDA Warns Healthcare Providers of Potential Rise in Death Rate With Impella RP
News Daily News

FDA Warns Healthcare Providers of Potential Rise in Death Rate With Impella RP

Caitlin E. Cox
Caitlin E. Cox
February 04, 2019
FDA Warns of Stroke and Arterial Dissection Risk With MS Drug
News Daily News

FDA Warns of Stroke and Arterial Dissection Risk With MS Drug

L.A. McKeown
L.A. McKeown
November 29, 2018
FDA Warns of Rising Endoleak Rates After Endovascular Aneurysm Repair
News Daily News

FDA Warns of Rising Endoleak Rates After Endovascular Aneurysm Repair

L.A. McKeown
L.A. McKeown
October 02, 2017
No More Absorb BVS: Abbott Puts a Stop to Sales
News Daily News

No More Absorb BVS: Abbott Puts a Stop to Sales

Caitlin E. Cox
Caitlin E. Cox
September 08, 2017
Absorb in Europe: When, How, and by Whom the Beleaguered BVS Is Being Used After Restrictions
News Features

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

Michael O'Riordan
Michael O'Riordan
May 08, 2017
TCTMD’s Top 10 Most Popular Stories for April 2017
News Daily News

TCTMD’s Top 10 Most Popular Stories for April 2017

Shelley Wood
Shelley Wood
April 28, 2017
Absorb BVS Use Restricted in Europe
News Daily News

Absorb BVS Use Restricted in Europe

Michael O'Riordan
Michael O'Riordan
April 06, 2017
News Daily News

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

L.A. McKeown
L.A. McKeown
January 31, 2017
News Daily News

Under Surveillance: Ballooning Numbers, Better Survival, Lower-Risk Patients in Latest TVT Registry Data

L.A. McKeown
L.A. McKeown
December 13, 2016

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