The DC Circuit ruled that the Librarian of Congress acted lawfully in permitting independent service organizations to bypass digital locks for medical device diagnosis, maintenance, and repair.
The FDA classified the action as a Class I recall after the manufacturer determined that some devices may not have received a previous firmware upgrade.
Certain procedure trays contain recalled sodium chloride ampules that may pose a risk of infection or organ failure.
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The agency released a discussion paper to address the unique risks and potential of generative artificial intelligence in the healthcare ecosystem.
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A survey of more than 300 professionals indicates that cybersecurity is a top concern as technical teams struggle with system complexity.
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A layered cybersecurity strategy can help healthcare organizations protect connected medical devices without disrupting clinical operations.
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Malicious attacks using artificial intelligence increased 56% over the previous year, according to the 2026 Cost of a Data Breach Report.
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The company reports no impact on manufacturing, patient services, or medical technology safety.
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The work group will develop playbooks and risk assessment tools to help healthcare organizations defend against advanced model risks.
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The collaboration provides health systems with evidence-based solutions to address medical device safety, infection control, and medication practices.
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The certification provides a framework for specific service lines and does not require prior organizational accreditation.
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The nonprofit organization named the California health system the winner of its 2026 Health Technology Excellence Award for a program that redistributes blood products.
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The nationwide recall affects Hudson RCI neonatal and infant heated wire breathing circuits following reports of melting, smoke, and localized thermal damage at the humidifier connector.
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The second phase introduces advisory services and a certification program to help hospitals maintain patient care during technology outages.
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