Amid an ongoing current of medical product recalls, hospitals in the United Kingdom are experiencing new electrical problems with certain Philips ventilators.
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Children who need a tracheostomy are at high risk of accumulating fluid behind their eardrum when on a ventilator, according to new research.
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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 guidelines to design mechanical ventilators that can work in low- and middle-income countries have been proposed, especially where few are available.
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ImtMedical, a subsidiary of Vyaire Medical, has initiated a recall of certain Bellavista ventilators, due to a software and configuration issue. The U.S. FDA cleared the BellaVista 1000e ventilator in late 2019.
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