(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 ...
Philips has been dealt another blow to its ventilator business after the US Food and Drug Administration (FDA) initiated another recall, due to a power malfunction that would cause its Trilogy EVO ...
Respironics, Inc., a Philips Healthcare business, today announced a worldwide recall of approximately 600 Philips Respironics Trilogy Ventilators, comprising Trilogy Ventilator Models 100, 200 and 202 ...
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 ...
Murraysville, Pa.-based Philips Respironics has issued a worldwide recall of its Trilogy Ventilators Models 100, 200 and 202 due to a potentially faulty component on the ventilators’ power boards. The ...
More than a year into the repair-and-replace program for the 5.5 million CPAP and BiPAP machines and other ventilators recalled by Philips since June 2021, the Dutch devicemaker has identified a pair ...
Just as Philips began plotting out its recovery from the Class I ventilator recall it’s been grappling with for the better part of a year, it was hit with another curveball. The Dutch devicemaker has ...
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