(Reuters) -The U.S. Food and Drug Administration (FDA) on Wednesday classified the recall of Philips' medical imaging devices as most serious as their use could cause serious injuries or death. The ...
Millions of Americans’ bedtime routine includes wearing a mask attached to a respiratory machine that pushes air into their lungs, supporting their breathing during sleep. These airway pressure ...
Though Philips has argued in court that its U.S. subsidiary should bear the sole responsibility of paying out damages related to its massive CPAP machine recall, instructions to continue selling ...
Koninklijke Philips N.V. (NYSE:PHG) has recalled some Panorama 1.0T HFO machines. The magnetic resonance (MR) system is used to take different kinds of images that show what's inside the body and can ...
The Food and Drug Administration issued a warning letter to Philips citing significant violations at three of its medical device facilities. The inspections took place between January and March 2025 ...
May 23 (Reuters) - When Philips Respironics in 2021 recalled millions of devices for treating sleep apnea, the company warned users of potential ill effects including kidney and liver damage in ...
This article originally appeared in ProPublica. ProPublica is a Pulitzer Prize-winning investigative newsroom. Sign up for The Big Story newsletter to receive stories like this one in your inbox. For ...
The U.S. Food and Drug Administration has issued a safety communication saying certain HeartStart automated external defibrillator devices made by Philips Medical Systems, a division of Philips ...
Some results have been hidden because they may be inaccessible to you
Show inaccessible results