FDA Gives Update on Philips Respironics Recalls

 Published: January 27, 2022

By: Addie Schiefer

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image of female health professional inspecting throat of young girl

The FDA has recently announced the recall of certain Trilogy EVO Ventilators for potential health risks from PE-PUR Foam. The FDA has identified this as a Class I recall, the most serious type of recall.

The FDA has provided an easy to read list of all products, model numbers, part numbers, and more that are being recalled. They’ve also included a more detailed reason for the recall, instructions on what to do, and who may be impacted. Read the full recall notice from the FDA

Email newsroom@aarc.org with questions or comments, we’d love to hear from you.

Addie Schiefer

Addie Schiefer is the Content Manager for the AARC where she creates engaging content for the association via the AARC website, newsletters, and social media. Connect with her about potential stories by email, AARConnect, or LinkedIn. When she’s not working, you can find her listening to a true crime podcast, traveling to new places with her husband, hanging out with her dog JoJo, or browsing the aisles of the nearest Target.

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