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.

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 ...

It’s been just over a year since Randy Boyd was diagnosed with cancer. In July 2020, he felt a bruise on the left side of his neck and went to the doctor. A biopsy revealed it was throat cancer. “I ...

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 ...

This is an archived article and the information in the article may be outdated.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

It’s been just over a year since Randy Boyd was diagnosed with cancer. In July 2020, he felt a bruise on the left side of his neck and went to the doctor. A biopsy revealed it was throat cancer. “I ...

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 ...