The use of in-line nebulizers placed in certain locations may lead to aerosol deposits forming over time on the ventilator flow sensor. Should this occur, there is a possibility of inaccurate flow ...
Smiths Medical is recalling its paraPAC Plus ventilators because of the possibility that the patient outlet connector could loosen or detach, affecting active ventilation. The FDA labeled the ...
90,905 ventilators recalled globally due to software errors causing potential safety risks. Nine injuries and one death reported; Philips requires urgent software updates. On Tuesday, Koninklijke ...
The FDA is elevating three sets of respiratory hardware recalls from Smiths Medical, covering portable ventilators and tracheostomy tubes that enter the airway through the neck. The agency ...