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 ...
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 ...
The Food and Drug Administration (FDA) has issued a recall of nearly 62,000 pacemakers that were distributed between April 2015 and February 2019 after it was discovered that moisture could get inside ...
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