More than a year after the official start of the ongoing Class I recall that has sent revenues plummeting and affected millions of CPAP and BiPAP machine and ventilator users around the world, ...

Though Philips recently expanded its ongoing respiratory device recall to include around 5.2 million machines, that list left off a handful of ventilators that weren’t affected by the original issue.

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Philips has called for urgent software updates and changes to nebulizer use for all Trilogy Evo Platform ventilators after the FDA flagged a serious safety risk. Using certain nebulizers can cause the ...

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Philips has issued a correction for Trilogy Evo Platform Ventilators, according to the U.S. Food and Drug Administration (FDA).

HARRISBURG, Pa. (WHTM) — Philips is recalling specific mechanical ventilators over concerns of possible carcinogenic effects. According to the U.S. Food and Drug Administration, specific Philips ...

Philips Respironics, Inc. has issued updated instructions for the use of its OmniLab Advanced+ (OLA+) Ventilator because of its demonstrated failure in the ventilator inoperative alarm that can cause ...

When you need a ventilator, finding a trusted source is a top priority. Whether you are a hospital preparing for a patient surge or a clinic looking for flexible rental solutions, knowing where to ...