The FDA has recalled Mercury Medical’s Neo-Tee T-Piece Resuscitator, a gas powered resuscitator intended primarily for ...

The Cybersecurity and Infrastructure Security Agency and Food and Drug Administration Jan. 30 released notices warning of ...

The FDA’s framework for AI regulation, while robust for premarket evaluation, would benefit from more specific mechanisms for continuous monitoring of AI performance in diverse real-world settings.

The backdoor on Contec CMS8000 patient-monitoring devices could allow an IP address at an unnamed university to remotely ...

Experts highlighted surgical robotics, artificial intelligence and M&A as top trends this year. However, the Trump administration could create challenges for the industry.

Vulnerabilities in certain Contec and Epsimed patient monitors can allow people to gain access and potentially manipulate the ...

What will the industry face or achieve in 2025? These trends will be critical in medical device cybersecurity.

The FDA says the cybersecurity vulnerabilities identified may put patients at risk when the device is connected to the internet.

CISA and FDA say Contec patient monitors used in the US contain a backdoor that could allow remote attackers to tamper with the device.

Today, the U.S. Food and Drug Administration (FDA) issued a safety communication to raise awareness about cybersecurity ...

Medical equipment maker Revvity forecast full-year profit and revenue for 2025 below Wall Street estimates on Friday, as it expects soft demand for its products and services used in drug research.

Journavx is designed to eliminate the risks of addiction and overdose associated with medications like Vicodin and OxyContin.