Philips Respironics has issued another ventilator recall deemed the most serious type by the FDA as it may cause serious injury or death.

Philips Respironics has removed certain DreamStation devices due to programming errors that can result in failed therapy modes, according to the U.S. Food and Drug Administration.

PHILLIPS HAS NOW RECALLED ALMOST 20 DIFFERENT MODELS OF CPAP AND BIPAP MACHISNE BECSEAU OF HEALTH CONCERNS. THE COMPANY SAYS THAT THE PHONE THAT IS INSIDE OFHE T MACHINES TO DAMPEN THE SOUND CAN BREAK ...

Here are four of the latest recalls and corrections reported to the FDA.

FORT WORTH (CBSNewsTexas.com) — A massive recall of millions of sleep apnea machines that has dragged on for nearly two years has left many patients waiting with seemingly no good options. In June of ...

CORPUS CHRISTI, Texas — As the number of COVID-19 cases in our country rise, supplies are dwindling. Medical professionals facing a shortage of ventilators in some areas of the country are turning to ...

Get all the latest news on coronavirus and more delivered daily to your inbox. Sign up here. As doctors face a shortage of ventilators that are crucial for treating coronavirus patients with ...