Philips sent updated instructions related to a problem with bilevel positive airway pressure, or BiPAP, machines that can cause interruption or loss of therapy. Philips recalled three models of BiPAP ...
The U.S. Food and Drug Administration on Friday announced the recall of certain Philips Respironics devices designed to help people with breathing conditions keep breathing at a regular rhythm. The ...
The Food and Drug Administration (FDA) sent a warning notice to Philips Respironics after patients and medical suppliers claimed they were unaware that certain breathing assistance machines had been ...
UPDATE (2024-07-05): Update on Philips Respironics recall of several models of CPAP and BiLevel PAP machines and mechanical ventilators Once consumers have completed the registration process, they ...
Millions of people across the country were jostled awake this year over fearful news: A critical device they were prescribed and relied on each night for sleep was suddenly labeled a hazard to their ...
AMSTERDAM, NETHERLANDS (NEWS10) – Philips Respironics has issued a recall on thousands of ventilators and CPAP machines. The recall only affects units sold in the United States. The units affected ...
Medical device maker Phillips formally entered into a consent decree that stops the company from selling sleep apnea machines in the United States over health concerns that include cancer. The decree ...
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