Lawmakers requested the report after a 2023 ProPublica and Pittsburgh Post-Gazette investigation revealed that the FDA had ...

(RTTNews) - Philips, in an update on earlier announced voluntary CPAP, BiPAP and Mechanical Ventilator recall notification, said Sunday that the US Food and Drug Administration recently conducted an ...

Technology company Philips plans to cut an estimated 5% of its workforce, about 4,000 positions, due to losses caused by the recall of a sleep apnea product as well as supply chain issues, according ...

Eight deaths and 13 injuries have been associated with a class I recall of Philips Respironics’ BiPAP ventilators. FDA noted that the devices may unexpectedly reboot or enter an interoperative state.

Medical device manufacturer Philips announced the company will expand on a previous recall in an ongoing effort to remove equipment that could have a contaminant in one of the plastic components.