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Some Philips CPAP, BiPAP machines may not work as intended, FDA says in recall

7 April 2023

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..

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Repaired sleep apnea machines could still pose serious health risks, FDA says

7 April 2023

Federal regulators are heightening their warning about devices made by Philips Respironics used to treat obstructive sleep apnea, saying the products "may cause serious injuries or death."

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