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The recall was issued due to the potential for the systems to produce artifacts during PET exams.

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Reducing the activity of a specific protein could provide significant relief for many heart failure patients.

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“Understanding how these national patterns manifest within radiology departments is critical for optimizing staffing, credentialing, and quality improvement initiatives,” authors of a new analysis in Academic Radiology contend.

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New findings suggest that the majority of older adults (65+) with lower risk head injuries do not have positive findings on CT imaging.

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Michael McKee is accused of making the journey from Illinois to Ohio and then shooting the two victims in their home on Dec. 30. He was arrested after surveillance footage showed his car at the scene before and after the murders. 

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Postprocedural gradients can tell cardiologists a lot about a patient's long-term risk of structural valve deterioration.

CGuard Prime carotid stent system was cleared by the U.S. Food and Drug Administration (FDA) in June 2025.

The CGuard Prime carotid stent system from InspireMD was approved by the FDA in 2025. These data confirm the device's ability to reduce a patient's stroke risk during treatment. 

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SIR, AdvaMed, Philips, Abbott and others in the Office-Based Facility Association contend more must be done to reverse these trends and protect private practices.

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The Missouri complaint mirrors those brought by the Federal Trade Commission, the state of Texas and Philadelphia-based Jefferson Health, among others, in that it’s focused on alleged collusion between pharmacy benefit managers and drug companies to control the price of insulin. 

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New data suggest that spending an extended period of time in a zero-gravity environment causes the brain to become somewhat displaced.

Vapor 2000 and Vapor 3000 devices manufactured by Draegar were improperly cleaned after parts were soldered on, meaning toxic metals could mix with medical gases. Due to the high risk posed to patient health, this recall has earned the FDA’s most serious designation. 

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Boston Scientific sent all known customers a letter on December 19, 2025 alerting them to an issue with certain AXIOS Stent and Electrocautery Enhanced Delivery Systems. During deployment, the stents may not expand. This can cause severe, potentially life-threatening injury to patients. All recalled stents must be removed from clinical settings immediately. 

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The recall was issued due to the potential for the systems to produce artifacts during PET exams.