House Hearing Exposes Critical Cybersecurity Risks in Medical Devices
MedPage Today
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Contributed by: Kate Gamble
Summary
A recent House hearing addressed the cybersecurity vulnerabilities of medical devices, particularly older models that may not comply with current standards. Rep. Gary Palmer emphasized the risks associated with aging technology and outdated software, noting that security issues have been highlighted by the FDA's warnings regarding patient monitors susceptible to unauthorized control. Concerns were raised about the impact of recent staff cuts at the FDA on its ability to enforce cybersecurity standards, with Rep. Yvette Clarke criticizing previous reductions that diminish the agency’s capacity to evaluate compliance with mandated improvements. Cybersecurity experts stressed the importance of a well-resourced workforce at the FDA to adapt to evolving cybersecurity threats in the medical device landscape.
