Baxter Permanently Removes Life2000 Ventilation System Due to Cybersecurity Issue
The company is pulling the Life2000 system from the market after finding a vulnerability that could allow unauthorized changes to ventilation settings.
The company is pulling the Life2000 system from the market after finding a vulnerability that could allow unauthorized changes to ventilation settings.
A state audit finds tens of thousands of ventilators and other devices purchased during COVID-19 remain unused and unmaintained.
CorVent Medical’s Respond ventilator, designed for pediatric to adult patients, has received FDA 510(k) clearance as the first U.S.-manufactured ventilator cleared in over 20 years.
The company is pulling the Life2000 system from the market after finding a vulnerability that could allow unauthorized changes to ventilation settings.
Three major manufacturers—Philips Respironics, Baxter Healthcare, and Zoll Medical—have issued Class I recalls for their ventilators due to critical issues posing a risk of serious injury or death.
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Read MoreMedtronic announced that it would exit the ventilator market that it characterized as increasingly unprofitable.
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The recall addresses potential risks that glued connections of breathing circuits may loosen either before or during the ventilation process.