The U.S. Food and Drug Administration (FDA) announced on June 3, 2022, that Philips Respironics would recall all V60 and V60 Plus ventilators. The FDA identified the Philips Respironics recall as a Class I recall, the most serious type of recall, for the potential to cause serious injuries or death. The products recalled as part … [Read more...] about Philips Respironics Recall Includes All v60 and V60 Plus Ventilators; FDA Categorizes Recall as Class 1