News Daily News Class I Recall for Certain Medtronic Pacemakers Due to Possible Circuit Error Todd Neale February 15, 2019
News Daily News FDA Warns Healthcare Providers of Potential Rise in Death Rate With Impella RP Caitlin E. Cox February 04, 2019
News Opinion Editor's Corner TCTMD’s Top 10 Most Popular Stories for January 2019 Caitlin E. Cox January 31, 2019
News Daily News Manufacturing Defect Leads to Recall of Implanted Medtronic CRT-D Devices, ICDs Todd Neale February 27, 2018
News Daily News FDA Warns Certain Zoll LifeVests Might Fail to Deliver Shocks Michael O'Riordan January 17, 2018
News Daily News Rivaroxaban Trial in Patients With Embolic Stroke of Undetermined Source Stopped Early Todd Neale October 09, 2017
News Daily News Abbott Vascular Recalls Three Coronary Catheters Because of Possible Sheath Removal Problems Todd Neale May 16, 2017
News Daily News Wingman35 Crossing Catheters Recalled Due to Tip Splitting, Separation Todd Neale May 04, 2017
News Daily News Boston Scientific Recalls All Lotus Valves, Including Lotus With Depth Guard Michael O'Riordan February 23, 2017
News Daily News Alirocumab to Remain On Market While Companies Clash Over Patents Michael O'Riordan February 09, 2017
News Daily News FDA Classifies Latest HeartWare VAD Recalls as Class I Michael O'Riordan October 24, 2016
News Daily News FDA Declines to Approve Portola’s Reversal Agent for Factor Xa Inhibitors Michael O'Riordan August 18, 2016
News Daily News FDA: Angiographic Catheter Recalled Due to Potential Tip Separation Todd Neale July 22, 2016
News Daily News FDA: No More Chances for Embattled Coagulation Monitoring System Todd Neale July 13, 2016
News Daily News FDA: No Más Oportunidades para el Acosado Sistema para Monitorizar la Coagulación Todd Neale July 13, 2016