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 ...

This is an archived article and the information in the article may be outdated. Please look at the time stamp on the story to see when it was last updated. (WKBN) – More than 17 million masks for ...

Nearly five years after the Philips Respironics recall reshaped the CPAP market, respondents to a recent HME Newspoll say ...

Certain Philips Respironics DreamStation breathing devices, commonly used for treating sleep apnea, may deliver the incorrect prescription or no therapy at all, the FDA warned in a recall announcement ...

The U.S. Food and Drug Administration has updated a recall affecting millions of Philips sleep apnea machines, now saying that they may been linked to at least 561 deaths. The agency, in a statement ...

Electronics manufacturing giant Philips is recalling millions of CPAP and BiPAP devices due to an issue that could potentially pose a health risk to users of the machines. In the wake of the recall, ...

CORPUS CHRISTI, Texas — If you have a CPAP or BiPAP machine that you no longer need there is a way to put it to good use during the COVID-19 pandemic. CPAP and BiPAP machines are generally used by ...

(WKBN) – More than 17 million masks for BiPAP and CPAP machines have been recalled, according to the U.S. Food and Drug Administration. The FDA said that Philips Respironics (Philips) has recalled ...