Philips will pay 288 million euros to settle an investigation related to its recall of millions of sleep and respiratory ...
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FDA issues highest-level recall for CPAP machines after defect found that can shut them off during sleep
The U.S. Food and Drug Administration has announced a Class I recall involving the BMC Medical Luna G3 APAP, model LG3600. Class I is the agency’s most serious recall classification, indicating that ...
SILVER SPRING, Md., April 9, 2024 /PRNewswire/ -- Today, the U.S. District Court for the Western District of Pennsylvania entered a consent decree of permanent injunction against Philips RS North ...
Philips has reached a settlement with the Department of Justice to tie up the remaining criminal and civil probes into its ...
Medical device company Philips announced a recall of millions of sleep apnea machines and ventilators because a material used inside them could put users at risk of cancer or other health issues.
A federal judge in Austin wants to know why a group of international investors is in Texas fighting for documents and testimony from an Austin-area doctor while the group is fighting for the same ...
WASHINGTON (AP) — The company behind a global recall of sleep apnea machines said Monday it will stop selling the devices in the U.S., under a tentative agreement with regulators that could cost the ...
The U.S. Food and Drug Administration (FDA) announced a recall on approximately 20,160 medical devices used to treat sleep apnea. This is due to a firmware defect. The device recalled is the Luna G3 ...
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