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Maker of recalled sleep apnea machines agrees to halt sales in U.S.
ProSomnus 510(k) Submission Under Review for Severe Indication
FDA rejected Philips Respironics' safety claims after CPAP recall but delayed telling public, emails show
FDA Repeatedly Rejected Safety Claims About Philips Breathing Machines, Emails Show — ProPublica
Amid recall crisis, Philips agrees to stop selling sleep apnea machines in the United States
Amid recall crisis, Philips agrees to stop selling sleep apnea machines in the United States
Philips' US sales of sleep apnea devices face years-long halt after FDA deal
Philips to halt sales of sleep apnea machines in US after global 2021 recall
FDA Requests More Tests on Royal Philips' Recalled Sleep Apnea Devices