On June 2, 2025, the Therapeutic Goods Administration (TGA), Australia’s medical device regulatory agency, started proceedings in the Federal Court of Australia against Philips for the alleged unlawful supply of medical devices that did not meet Australian safety and performance requirements. These included devices used by people with sleep apnea at home and other devices […]
By Sree Roy The Philips recall has clearly influenced CPAP prescribing habits, according to new survey data from Sleep Review. The survey highlights how sleep physicians are navigating patient-facing device features, sound abatement technology, and patient adherence strategies four years after the Philips CPAP recall disrupted the market. Impacts of Philips CPAP Recall Physicians who […]
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