FDA OKs Inogen Simeox 200 Airway Clearance Device
The Inogen Simeox 200 Airway Clearance Device aids bronchial drainage in patients with chronic respiratory conditions using high-frequency oscillatory vibrations and intermittent negative pressure.
The Inogen Simeox 200 Airway Clearance Device aids bronchial drainage in patients with chronic respiratory conditions using high-frequency oscillatory vibrations and intermittent negative pressure.
Hamilton Medical issued a software correction for the Hamilton-C6 ventilator due to a failure to restart ventilation in sensor fail mode.
The recall addresses potential risks that glued connections of breathing circuits may loosen either before or during the ventilation process.
The Inogen Simeox 200 Airway Clearance Device aids bronchial drainage in patients with chronic respiratory conditions using high-frequency oscillatory vibrations and intermittent negative pressure.
New findings may help guide policy makers in deploying ventilators to states with an urgent need of the technology.
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Read MoreThe Draeger SafeStar 55 has been identified by the U.S. FDA as a Class I recall, the most serious type of recall.
Read MoreThe Canadian government’s response to ventilator needs of patients early during the pandemic resulted in an excessive equipment surplus.
Read MoreBaxter has issued an Urgent Medical Device Correction for the home care Volara System to reinforce important safety information.
Read MoreRussia’s invasion of Ukraine has intensified concerns of global cyberattacks on critical medical devices, such as ventilators, which are being targeted by cybercriminals in the U.K.
Read MoreIntuitive measures to curb the initial unpreparedness for the pandemic resulted in the inflow of mechanical ventilators at the expedited rate.