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Novartis sued for allegedly leaking data on breast cancer patient to Google, Contentsquare
More than 80% of clinicians have had to correct AI-supplied misinformation during patient visits: New patient + provider survey
CMS leaves the ’80s behind with shift away from snail mail correspondence, fax machines
Drugmaker’s stock tumbles 20% after FDA issues formal warning to executives
6 things Medicaid stakeholders can remind the world to always do with healthcare AI
voice audio recording smartphone
FDA sees promise in voice-based AI model for heart failure

An advanced algorithm that looks for signs of heart failure in five-second voice recordings has received the FDA's breakthrough device designation.

Medtronic’s MiniMed 780G automated insulin delivery system
Software errors lead to major insulin pump recall—manufacturer shares a fix

Nearly 27,000 MiniMed 780G insulin pumps were included in a new Class II recall. By taking a few basic steps, however, patients should be able to avoid any significant risks.

UnitedHealth Group - 2
Activist investors sue UnitedHealth to force annual reporting on patient care access

Led by a Quebec-based faith organization, a coalition of investors is asking a court to force UnitedHealth to provide details on the social impacts of its history of mergers and acquisitions. The lawsuit comes after the plaintiffs, all company shareholders, failed to get the proposal passed through internal channels. The Securities and Exchange Commission has also opted not to intervene. 

happy pill time
ChatGPT is penetrating healthcare with explosive might, a US state is trying human-less prescription refills—and more AI news not to miss

If you still think of large-language AI as a newish thing yet to catch on with healthcare consumers, think again.

Family of woman wrongly declared dead receives $3.3M settlement

Timesha Beauchamp, 20, suffered a seizure in August 2020 that required emergency medical attention. When responders arrived, they declared her dead at the scene. A short time later, she was found to be alive at a funeral parlor. More than five years later, a lawsuit stemming from the incident has been settled out of court. 

the words "FDA recall" on a board
FDA issues Class I recall on B. Braun microbore extensions due to risk of death

The extensions are used to supply patients with fluids and drugs through an IV line. Despite being labeled as having them, the devices do not contain an air-eliminating vent. Because there is a serious risk of air embolism associated with the error, the FDA has given this recall its most serious designation.

Trump and Robert F. Kennedy Jr., secretary of health and human services (HHS). White House press photo
Is RFK Jr. really conducting an ‘assault on vaccines’? And more high-level news notes

The CDC has gone ahead and changed its recommendations for childhood immunizations. The gnashing of teeth has only just begun. 

U.S. FDA Sign
FDA recalls surgical packs due to risk of microbial contamination

Multiple lots of ophthalmic surgery packs manufactured by Alcon will need to be disposed of, due to an incomplete seal that could cause the sterile bandages and syringes inside to be compromised. Because of the serious health risk posed to patients, this recall has been designated Class I. 

the words "FDA recall" on a board
FDA confirms new recall after catheter sheath was left in patient’s body

This is a Class I recall, which means the FDA believes these devices could cause a serious injury or death.

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Cardiovascular Business
Catheter-based treatment linked to major benefits for intermediate-risk PE

New 30-day data presented at ACC.26 helped answer questions cardiologists have had been asking for years. “Thank you for bringing PE into the future," one vascular specialist said from the stage.