The US Food and Drug Administration issued a Class I recall Friday, the most serious type of recall, for certain Philips Respironics DreamStation1 CPAP machines. A Class I recall means the FDA has ...
Koninklijke Philips PHG is recalling some Bi-Level Positive Airway Pressure (Bi-Level PAP), Continuous Positive Airway Pressure (CPAP), and mechanical ventilator devices in the United States, as ...
Over 560 deaths have been reported in connection with recalled Phillips devices designed to treat sleep apnea and other breathing disorders, the Food and Drug Administration (FDA) reports. Since April ...
AMSTERDAM (Reuters) -Dutch medical equipment company Philips has recalled some breathing devices and ventilators because of a foam part that might degrade and become toxic, potentially causing cancer, ...
An urgent recall has been issued for about four million ventilators and sleep apnoea machines that can leech toxic particles into organs and cause cancer. Breathing aids manufactured by Dutch ...
Royal Philips has issued a recall for some of its ventilator and breathing machines due to a health risk that could cause cancer. The company issued the notice for specific Philips Bi-Level Positive ...
Jeffrey Reed, who experienced persistent sinus infections and two bouts of pneumonia while using a Philips CPAP machine, poses with the device at his home Thursday, Oct. 20, 2022, in Marysville, Ohio.
Consumer Affairs in partnership with Environmental Health have undertaken the necessary recall procedures following the recall of Philips Respironics sleep and respiratory care devices. A Government ...
AMSTERDAM (Reuters) -Dutch medical equipment company Philips has recalled some breathing devices and ventilators because of a foam part that might degrade and become toxic, potentially causing cancer, ...
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