An FDA recall has been issued for the Bunnell Life Pulse high frequency ventilator patient circuits, according to the American Society of Anesthesiology.
The patient circuit, which provides a channel for humidifying, warming and temperature monitoring gas, is at risk for melting heater wire insulation. The melting can cause sparking and smoke, which has potentially lethal side effects.
Affected circuits were distributed after March 19, 2012 through October 2012.
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The patient circuit, which provides a channel for humidifying, warming and temperature monitoring gas, is at risk for melting heater wire insulation. The melting can cause sparking and smoke, which has potentially lethal side effects.
Affected circuits were distributed after March 19, 2012 through October 2012.
More Articles on Anesthesia:
Ventlab's Manual Resuscitators Recalled by FDA
CMS Prepares for Mandated 27% Sustainable Growth Rate Cut in 2013
Anesthesia Participation in Meaningful Use Could be Eased by Proposed Legislation