Draeger Breathing Filter Gets Class I Recall
The Draeger SafeStar 55 has been identified by the U.S. FDA as a Class I recall, the most serious type of recall.
The Draeger SafeStar 55 has been identified by the U.S. FDA as a Class I recall, the most serious type of recall.
Amid an ongoing current of medical product recalls, hospitals in the United Kingdom are experiencing new electrical problems with certain Philips ventilators.
Bothell, Wash.-based Ventec Life Systems announces that its standalone V+Pro ventilator is reimbursable.
The Draeger SafeStar 55 has been identified by the U.S. FDA as a Class I recall, the most serious type of recall.
Although allocation guidelines for mechanical ventilatory support are essential in a public health emergency, only 26 US states provided public guidance on how this allocation should occur.
Read MoreThe U.S. FDA has granted Denver, N.C.-based BioMedInnovations, LLC, an Emergency Use Authorization (EUA) to manufacture and distribute SuppleVent, the company’s back-pressure regulator-based ventilator technology.
Read MoreVentilator shortages in COVID-19 hotspots have forced some emergency physicians to do what was once unthinkable: modify the equipment to accommodate more than one patient simultaneously. But is that a good idea?
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