WebDec 20, 2024 · That’s why it’s important to know if any recalls exist for a device you use, like a CPAP. Currently, there is a recall for the Philips Respironics CPAP and BiPAP devices. The U.S. Food and Drug Administration ( FDA) issued a recall for these devices from Philips Respironics in June 2024: E30. DreamStation ASV. WebPhilips Respironics announced a voluntary recall of millions of certain CPAP, BiLevel PAP, and ventilator devices because there are issues with the sound abatement foam used in these devices. As the foam degrades over time, it has been found to have the potential to expose users to possible carcinogens and toxic chemicals that can be off-gassed.
Philips Respironics CPAP, BiPAP, and Ventilator Recall: FAQs
WebContact and support options for patients impacted by the June 2024 voluntary recall of certain CPAP, BiPAP and mechanical ventilators related to PE-PUR sound abatement foam. Please note, dependent on which customer care team you need to speak with, we may be experiencing a high volume of calls and wait times may be longer than normal. WebMar 31, 2024 · The following products listed are affected by the recall notification / field safety notice: CPAP and BiLevel PAP Devices All Affected Devices Manufactured Before 26 April 2024, All Device Serial Numbers Continuous Ventilator, Minimum Ventilatory Support, Facility Use E30 (Emergency Use Authorization) Continuous Ventilator, Non-life Supporting from the earth brewing menu
Recall Information for Healthcare Professionals - ResMed
WebDec 6, 2024 · An update from ResMed’s CEO: Here at ResMed, the leading global manufacturer in sleep apnea therapy, we know that ongoing treatment is critical to the … WebSep 9, 2024 · Manufacturer facing legal challenges from previous recall. The FDA issued a notice in June 2024 advising that Philips recalled certain BiPAP, and CPAP machines due to risk of degrading foam ... from the earth marijuana dispensary