Philips CPAP & BiPAP Recall
The Philips CPAP lawsuits claim the use of various Philips CPAP machines can cause lung injuries and
On June 14, 2021, Philips announced a voluntary recall for various Philips Bi-Level Positive Airway Pressure (Bi-Level PAP), Continuous Positive Airway Pressure (CPAP) & mechanical ventilator devices.
On July 22, 2021, the FDA issued an official Class 1 recall of numerous Philips CPAP Machines. As noted by the FDA, a class 1 recall is “the most serious type of recall. Use of these devices may cause serious injuries or death.”