News Daily News FDA Provides Update on Poorer Survival With Impella RP in Postmarket Setting Todd Neale May 21, 2019
News Daily News FDA Provides Update on Tainted ARB Investigation, With New Impurity Found Todd Neale March 04, 2019
News Daily News Some Stryker Defibrillators Under Recall for ‘Freezing’ Issue Todd Neale February 27, 2019
News Daily News Class I Recall for Certain Medtronic Pacemakers Due to Possible Circuit Error Todd Neale February 15, 2019
News Daily News More INR Test Strips Recalled Due to Inaccurately High Results Todd Neale December 21, 2018
News Daily News HeartMate 3 Problem With Outflow Graft Twisting Called Class I Recall by FDA Todd Neale May 23, 2018
News Daily News FDA: Battery, Cybersecurity Issues With ICDs and CRT-Ds Now Have Firmware Fix Todd Neale April 17, 2018
News Daily News Manufacturing Defect Leads to Recall of Implanted Medtronic CRT-D Devices, ICDs Todd Neale February 27, 2018
News Daily News Rivaroxaban Trial in Patients With Embolic Stroke of Undetermined Source Stopped Early Todd Neale October 09, 2017
News Daily News Penumbra Stent Retriever Recalled Due to Potential for Wire to Break, Separate Todd Neale July 21, 2017
News Daily News Inferior Vena Cava Filter Use Fell After FDA Warning but Remains High Todd Neale July 12, 2017
News Features Catheter Kerfuffle: How Concerning Is Off-Label Use in Stroke Interventions? Todd Neale June 21, 2017
News Daily News HeartMate II Left Ventricular Assist System Under Recall Due to Controller Exchange Problems Todd Neale May 24, 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 Recall Underway for AED Electrodes With Compatibility Problems Todd Neale October 17, 2016