Medical device companies navigating regulatory pathways should know: Large language models are not reliable guides. 

Almost one in three healthcare organizations allow their people to use AI without formal restrictions. 

Dermatologists increasingly rely on medical imaging modalities—especially but not solely ultrasound—to help diagnose complex and diverse skin disorders. 

Philips is recalling all sizes of its Tack Endovascular System after 20 patient injuries were reported. Interventional cardiologists are urged to stop using the device immediately. 

The American College of Cardiology and American Heart Association published the new guidelines with assistance from other leading U.S. medical societies. 

The recall impacts products from ROi, supplied by Mercury Medical. A defective spring can cause a controller to malfunction, resulting in poor ventilation. 

While there have been no reported deaths, certain lots of Olympus single-use guide sheath kits are to be quarantined immediately. 

Those involved plan to hire a community health worker and care navigator to help shepherd underserved patients through the screening process.