(RTTNews) - Philips Respironics, affiliated to Dutch consumer electronics giant, announced additional usage instructions for Trilogy Evo Ventilators related to use of in-line nebulizers. The company ...
90,905 ventilators recalled globally due to software errors causing potential safety risks. Nine injuries and one death reported; Philips requires urgent software updates. Memorial Day Special: Access ...
FDA today identified Philips Respironics Trilogy Evo continuous ventilator recall as Class I, over a month after the company initiated the voluntary correction in March. The ventilators affected by ...
Philips Respironics Inc., of Murrayville, Pa., was compelled to engage in multiple recalls over the use of a supplier’s polyester-based polyurethane (PE-PUR) sound abatement foam, and the latest ...
FILE PHOTO: The logo of Dutch technology company Philips is seen at the company headquarters in Amsterdam (Reuters) -The U.S. Food and Drug Administration (FDA) on Wednesday classified an expanded ...
In March, Philips recalled more than 73,000 ventilators that absorbed dust and dirt into breathing tubes. This week, the Food and Drug Administration reported that the issue has been associated with ...
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