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

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

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

Last week, the US Court of Appeals for the Fourth Circuit in United States v. Jackson upheld a doctor’s conviction under Section 301(k) of the ...

Among the wave of guidance documents issued by the U.S. Food and Drug Administration (“FDA” or the “Agency”) in the first week of 2025 were ...

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

Following the Trump administration's DEI ban, the FDA's move to scrub webpages has ensnared many pages focused on ensuring ...

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

The FDA is urging Congress to implement mandatory medical device shortage reporting to address growing vulnerabilities in the ...

In its most recent effort to keep pace with advancing technology, the US Food and Drug Administration (FDA) recently issued ...

The website changes raise concerns about “the interference of politics with the study and the practice” of science and ...

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