Customers were making numerous complaints about black debris or particles in the airpath circuit of their mechanical ventilators, BiPAP, and CPAP devices.
The FDA issued a Class I Recall for the devices, the most serious type of recall for CPAP and BiPAP devices, as well as a series of mechanical ventilators manufactured and sold by Philips Respironics.
On June 14, 2021 Philips Respironics issued a recall and notified customers of the defective CPAP devices.
If you used one of these devices... Act Now!