4 results

• Philips Trilogy Evo Ventilator Recall Issued After Serious Injuries Reported

  April 17, 2026

  Martha Garcia

  The FDA has declared that a Philips Trilogy EVO ventilator device correction should be considered a class I recall, saying the problems are capable of causing serious injury or death following three injury reports.

• Philips Ventilator Recall Issued Due to Aerosol Deposits From In-Line Nebulizer Placements

  November 21, 2024

  Irvin Jackson

  The FDA has determined that urgent correction letters sent out by Philips to address problems with oxygen flow in certain ventilators constitutes a class I recall, meaning the agency believes the problems can result in serious patient injuries or deaths.

• Philips Recalls Trilogy Evo Ventilators for Lung Injury Risks When Used With Nebulizers

  October 8, 2024

  Darian Hauf

  Philips Respironics has issued a recall of several Trilogy Evo ventilator models used in conjunction with nebulizers over the risk of device malfunctions and lung injuries.

• Philips Trilogy EVO Ventilator Recall Issued Due to Software-Related Power Malfunction Risk

  May 14, 2024

  Irvin Jackson

  About 100,000 Trilogy EVO ventilators are being recalled due to a software error which can lead to the devices ceasing to function for patients in need of life-saving oxygen supplementation.