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An NIH-supported study found that an AI model analyzing single-lead ECG signals and sleep-stage data could sort patients by long-term cardiovascular risk, but it is not yet a clinical screening…
The FDA issued a potentially high-risk early alert for Philips Lumify diagnostic ultrasound systems after reports of unexpected loss of scanning capability, eight serious injuries and four deaths.
A new FDA final rule lets manufacturers use salt substitutes in foods governed by standards of identity, creating more flexibility to reduce sodium without requiring companies to reformulate.
HHS opened an NIH clinic for health problems reported after vaccination and announced proposed physician reimbursement, electronic-record requirements and a VAERS modernization.
A federal jury convicted a Florida laboratory executive and marketer over a scheme that billed Medicare more than $15 million for unwanted blood tests.
Leader Formulas recalled one lot of RAPTURE pre-workout after FDA testing found DMAA. The products were sold nationwide in three flavors from January 2025 through May 2026.
WHO's first global childhood-obesity guidance prioritizes nutrition, activity and behavioral support, with medicines and surgery reserved for limited cases.
An analysis of more than 85 million U.S. adult records found the sharpest drop in shingles diagnoses among the first birth cohort eligible for routine childhood chickenpox vaccination.
Kenya confirmed its first imported Bundibugyo Ebola case after a traveler from Congo died in Nairobi. Contacts are being monitored, and WHO says no travel restrictions are recommended.
A federal appeals court heard arguments over an order blocking 13 Kennedy appointees from the CDC vaccine advisory panel. The judges did not rule Tuesday.