The US Food and Drug Administration (FDA) is reminding healthcare providers about the risk of major complications if cardiac perforation occurs during leadless pacemaker implantation. Cardiac ...
With more self-contained models potentially on their way to patients, the FDA is taking steps to remind healthcare providers of certain risks posed by leadless pacemakers, including the possibility of ...
Background: Patients over the age of 75 represent more than half the recipients of permanent pacemakers. It is not known if they have a different risk of complications than younger patients. Methods: ...
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 ...
Engineers developed the smallest pacemaker yet: a device smaller than a grain of rice, activated by light, and meant to dissolve after it has met the patient's need for temporary pacing. (Nature) FDA ...
Dr. Srihari S. Naidu speaks with Parade to answer all our questions about pacemakers.
Some results have been hidden because they may be inaccessible to you
Show inaccessible results