Baxter is replacing faulty battery chargers in the Life2000 Ventilator system after identifying a defect that triggers alarms and renders the device inoperable.
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Philips has updated instructions for several ventilators to address aerosol deposits on internal sensors when used with in-line nebulizers.
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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.
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Nihon Kohden ventilators have obtained ATO certification under the DoD’s Risk Management Framework for cybersecurity.
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GE HealthCare has issued an update to the EVair Compressor recall, with testing results confirming safe usage across all patient groups.
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