The FDA has updated its guidance on GE HealthCare’s EVair compressor, confirming that formaldehyde emissions are within safety limits, while previous recommendations remain in place for the EVair 03 (Jun-Air) compressor.
The FDA has updated its guidance on GE HealthCare’s EVair compressor, confirming that formaldehyde emissions are within safety limits, while previous recommendations remain in place for the EVair 03 (Jun-Air) compressor.
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GE Healthcare is recalling Carescape R860 ventilator backup batteries, including replacement backup batteries, because the batteries may run out before they are expected to do so, according to an FDA advisory.
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GE Healthcare is recalling some Carescape Respiratory Modules and Airway Gas Option due to a manufacturing issue which may cause the devices to display incorrect oxygen values, according to an alert from the FDA.
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Last fall, GE Healthcare released its newest critical care ventilator to European markets, the Carescape R860.
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