Philips Respironics issued another recall on some of its respiratory machines due to a plastic component that could potentially be contaminated with a non-compatible material. The U.S. Food and Drug ...

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 ...

(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 ...

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 ...

Philips Respironics recalled more than 17 million masks used with their continuous positive airway pressure, or CPAP, and bilevel positive airway pressure, or BIPAP machines. The Food and Drug ...

In a classic “two steps forward, one step back” situation, just as Philips is aiming to wrap up the repair-and-replace program for the 5.5 million respiratory devices it began recalling two years ago, ...

This is an archived article and the information in the article may be outdated.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 ...