Respironics has issued additional usage instructions as part of a voluntary recall of some of its ventilators.

Philips recalls 90,905 ventilators globally due to software malfunctions affecting patient safety. The FDA warns of serious ...

Philips Respironics, affiliated to Dutch consumer electronics giant, announced additional usage instructions for Trilogy Evo ...

Trilogy Evo O2 and Trilogy Evo Universal models. The agency labeled the recall effort as Class I, its most serious, though no devices need to be returned to the manufacturer. The FDA said it has ...

Philips Respironics has issued a voluntary correction for Trilogy Evo, Trilogy Evo O2, Trilogy Evo Universal and Trilogy EV300 ventilators regarding the use of in-line nebulizers.

Philips also said it added missing contraindications in the devices’ instructions for use, and fixed translation errors in instruction manuals in Korean, Traditional Chinese and Spanish. Philips began ...