News Daily News FDA: Class I Recall for Burst Balloons With Sapien 3 Ultra Delivery System Michael O'Riordan August 22, 2019
News Features Wearables Under the Microscope: How New Tech Will Disrupt Patient-Physician Dynamics Marcus A. Banks August 15, 2019
News Daily News New Recall for Maquet/Datascope IABPs Due to Potential Battery Failure Marcus A. Banks July 24, 2019
News Daily News Burst Balloons With Sapien 3 Ultra Prompt ‘Urgent Field Safety Notice’ and Canadian Recall Shelley Wood July 22, 2019
News Daily News FDA: Class I Recall for IntraClude Intra-Aortic Occlusion Device Shelley Wood July 02, 2019
News Daily News FDA Class I Recall for PTA Catheters Due to Unexpected Balloon Bursting Yael L. Maxwell June 18, 2019
News Opinion Editor's Corner TCTMD’s Top 10 Most Popular Stories for May 2019 Caitlin E. Cox May 31, 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 FDA Provides Update on Poorer Survival With Impella RP in Postmarket Setting Todd Neale May 21, 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 Warns of Premature Battery Depletion With Certain Medtronic Pacemakers Michael O'Riordan May 07, 2019
News Daily News Two Pediatric Cardiac Catheters Recalled for Defective Balloons L.A. McKeown April 26, 2019
News Daily News FDA Warns of Cybersecurity Vulnerabilities With Some Medtronic Implanted Devices Michael O'Riordan March 22, 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