In a safety communication dated December 16 posted to the site of the FDA, the agency stated: “The U.S. Food and Drug Administration is alerting patients, caregivers, and health care providers about ...

Researchers have examined long-term outcomes in patients who received pacemaker implantations after transcatheter aortic valve replacement through their groin. The result showed no significant ...

Needing a permanent pacemaker after surgical aortic valve replacement (SAVR) was linked to mortality in Swedish registry data. Such risk was not apparent in the first few years: all-cause mortality ...

Patients who undergo minimally invasive heart valve replacement, known as TAVR, sometimes develop heart rhythm problems that necessitate placement of a permanent pacemaker. However, when a pacemaker ...

Paris, France and Munich, Germany, December 21, 2023 – TRiCares SAS (“TRiCares”), a privately held pioneer in the field of minimally invasive treatment of tricuspid regurgitation, today is pleased to ...

Editor's Note: The U.S. Food and Drug Administration classified Guidant's action as a class 1 recall on July 22, 2005. July 19, 2005 — Guidant Corp. has warned healthcare professionals and consumers ...