Philips Respironics Recall Includes All v60 and V60 Plus Ventilators; FDA Categorizes Recall as Class 1
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
Philips CPAP, BiPAP, and Ventilator Lawsuits
Philips Respironics CPAP, BiPAP, and Ventilator Machines Recalled for Potentially Deadly Product Degradation Those who are using a Philips CPAP or BiPAP for sleep apnea are urged to check their breathing machine to see if the unit is part of the 2 million unit recall. According to a Food and Drug Administration (FDA) notice, … [Read more...] about Philips CPAP, BiPAP, and Ventilator Lawsuits
