Delaware Business Now
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A consumer alert has been issued for users of respiratory devices manufactured by Philips. An estimated 4 million Philips Continuous Positive Airway Pressure (CPAP) and Bi-Level Positive Airway Pressure (BiPAP or BiLevel PAP) devices, as well as mechanical ventilators manufactured before April 26, 2021.
The recalls are due to potential health risks associated with the sound abatement foam in the devices.
The Delaware Department of Insurance announced that it issued the notice after the company’s recall notification and what it views as a lack of communication to consumers and facilities.
Recalled devices include those listed as providing respiratory treatment or support for Covid-19 patients. CPAP devices are used by individuals who suffer from sleep apnea, a disorder that leads to a temporary stop to breathing during sleep and can lead to death.
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