(RTTNews) - Philips Respironics, affiliated to Dutch consumer electronics giant, announced additional usage instructions for Trilogy Evo Ventilators related to use of in-line nebulizers.

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.

It is the second Class 1 recall issued for one of the company's ventilators in the past year and covers Trilogy models 100, 200 and 202. In June 2013, Respironics recalled 19,000 V60 devices due ...

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.

MURRYSVILLE, Pa., July 17, 2012 /PRNewswire/ --Respironics, Inc. announced today that it is voluntarily recalling 80 Trilogy Model 100 and five Trilogy Model 202 ventilators in the United States.

Philips Respironics initiated a voluntary recall to address a potentially defective component on the Trilogy Ventilator power management board, which could affect the function of the device.

Philips Respironics, a division of Philips Healthcare, has initiated a voluntary recall of its Trilogy Ventilator to address a potentially defective component on its power management board.

The U.S. Food and Drug Administration has ordered a software recall for a type of ventilator, for fear of "serious injuries or death."The ventilators—the Philips Respironics, Inc. 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 ...

MURRYSVILLE, Pa., Feb. 19, 2014 /PRNewswire/ -- Respironics, Inc., a Philips Healthcare business, today announced a worldwide recall of approximately 600 Philips Respironics Trilogy Ventilators ...