Philips Respironics, affiliated to Dutch consumer electronics giant, announced additional usage instructions for Trilogy Evo ...
Respironics has issued additional usage instructions as part of a voluntary recall of some of its ventilators.
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.
The use of in-line nebulizers placed in certain locations may lead to aerosol deposits forming over time on the ventilator flow sensor. Should this occur, there is a possibility of inaccurate flow ...
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Philips recalls 90,905 ventilators globally due to software malfunctions affecting patient safety. The FDA warns of serious ...
The FDA is getting the word out on a mandatory software update from Philips for its Trilogy line of portable life support ventilators, used in both hospitals and the home. Philips’ Respironics ...
Recommended Reading ‘An incredible undertaking’: 5 takeaways from Philips consent decree Philips recalled several models of its Trilogy ventilators because of multiple problems that can result ...
A spokesperson for the FDA said: “On March 19, 2024, Philips Respironics sent all affected ... especially across its Trilogy EVO line which was already subject to a previous class I recall ...
Philips’ Trilogy ventilators provide breathing support in medical ... “The notice also includes information on labeling and instruction manual updates. Philips Respironics is also addressing new ...