(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 ...
Americans cannot rely on the Food & Drug Administration (FDA) to guarantee that medical devices are safe, and a recent Government Accountability ...
Philips faces significant challenges and controversies, including the results of a forced recall of ventilators and respiratory devices, leading to financial provisions and damage to its brand ...
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 ...
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 ...
Royal Philips received a letter from the Food and Drug Administration warning that some of the medical device maker's facilities don't comply with federal manufacturing regulations. The warning letter ...
LONDON (MarketWatch) -- Royal Philips Electronics NV, Europe's largest maker of consumer electronics, on Monday reported a sharp decline in third-quarter profit, reflecting the sale of its ...
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