Philips’ Ventilator Woes Drag on with Yet Another Class I Recall
The U.S. FDA announced a Class I recall—the most serious type of recall—for the Philips Respironics V60 and V60 Plus Ventilator.
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New Bipartisan Legislation Spurs Right to Repair Campaign’s Momentum
The bipartisan measure, like bills pending in state houses around the country, would require manufacturers to provide access to the parts, tools, and information needed to fix products.
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ECMO May Offer Sickest COVID Patients Significant Lung Recovery, Study Finds
Patients with severe COVID-19 who are treated with extracorporeal membrane oxygenation (ECMO) may experience significant lung recovery.
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ECRI Names Staffing Shortages, Clinician Mental Health Top Patient Safety Threats
Staffing shortages and the mental health of healthcare workers topped a list of current patient safety concerns released by ECRI.
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FDA Orders Philips to Notify Patients of Recall of Certain Breathing Assistance Machines
The FDA issued a notification order to Philips Respironics requiring the company to of the recall of certain breathing assistance machines.
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