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State Insurance Department highlights recall of ventilators and CPAP devices

Delaware Business Now Reading Time: 2 minutes 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.

SHAREHOLDER ALERT: Pomerantz Law Firm Investigates Claims On Behalf of Investors of Koninklijke Philips N V

Share this article Share this article NEW YORK, June 22, 2021 /PRNewswire/  Pomerantz LLP is investigating claims on behalf of investors of  Koninklijke Philips N.V. ( Philips or the Company ) (NYSE: PHG).  Such investors are advised to contact Robert S. Willoughby at [email protected] or 888-476-6529, ext. 7980. The investigation concerns whether Philips and certain of its officers and/or directors have engaged in securities fraud or other unlawful business practices.  On June 14, 2021, Philips issued a voluntary recall of certain of its Bi-Level Positive Airway Pressure (Bi-Level PAP) and Continuous Positive Airway Pressure (CPAP) devices, as well as mechanical ventilators, after finding that the sound abatement foam used in the devices can degrade and become toxic, potentially causing cancer. 

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