According to the NIH, about 1.6 million people in the U.S. suffer from a condition where the tricuspid valve does not properly close ...

The Food and Drug Administration (FDA) has cleared the Jewel ® Patch Wearable Cardioverter Defibrillator (Patch-WCD) for adult patients aged 18 years and older who are at risk for sudden cardiac ...

Discover how The Memory Wave by Binaural Technologies blends Miracle Sound Frequency Activation, gamma wave entrainment, and ...

BrightHeart has its second FDA clearance for updates to its platform, an AI-powered digital screening tool for congenital ...

Another day, another recall — this time, a massive FDA recall of more than 4,500 cases of Yellowstone-inspired baked beans due to the presence of undeclared soy. Soy is a major allergen and ...

Major adverse events remained common in patients with nonischemic cardiomyopathy implanted with an electronic device. Image: Adobe Stock At Heart Rhythm 2025, Valentina Kutyifa, PhD, MD ...

A woman who had a spinal cord stimulator implanted in 2020 is suing devicemaker Boston Scientific and the FDA over complications she experienced with the device. Dena Lawler received the Spectra ...

Here’s what you need to know about the recall. Why is the FDA recalling certain tattoo ink ... Tattoo Ink” on top of an illustrated human heart. What should consumers who are looking to ...

This week, the U.S. Food and Drug Administration (FDA) announced two ongoing recalls on fresh tomatoes due to potential salmonella contamination. Here's what you need to know. The first recall was ...

The US Food and Drug Administration has approved the first at-home self-collection device for cervical cancer screening in the United States, called the Teal Wand, according to the women’s ...