News Daily News FDA Deems ‘Field Action’ for Faulty IABPs a Class I Recall Shelley Wood August 07, 2017
News Features Catheter Kerfuffle: How Concerning Is Off-Label Use in Stroke Interventions? Todd Neale June 21, 2017
News Opinion Editor's Corner TCTMD’s Top 10 Most Popular Stories for May 2017 Shelley Wood June 01, 2017
News Daily News FDA: Class I Recall for Over 47,000 HeartStart MRx Monitor/Defibrillator Units L.A. McKeown March 24, 2017
News Conference News ACC 2017 FDA Warns of Risk of Major Adverse Cardiac Events With Absorb BVS Michael O'Riordan March 18, 2017