Medical Device Recall Information - Philips Respironics Sleep and ...
In June 2021, after discovering a potential health risk related to the foam in certain CPAP, BiPAP and Mechanical Ventilator devices, Philips Respironics issued a voluntary Field Safety Notice …
Recalled Philips Ventilators, BiPAP Machines, and CPAP Machines
2024年11月20日 · In June 2021, Philips Respironics (Philips) recalled certain ventilators, bi-level positive airway pressure (also known as Bilevel PAP, BiPAP, or BPAP) machines, and …
Foam Testing Summary for Recalled Philips Devices
2024年8月15日 · In June 2021, Philips Respironics (Philips) recalled certain ventilators, bi-level positive airway pressure (also known as Bilevel PAP, BiPAP, or BPAP) machines, and …
FDA Activities Related to Recalled Philips Devices
2024年11月20日 · On June 30, 2021, the FDA alerted people who use certain Philips Respironics (Philips) ventilators, bi-level positive airway pressure (also known as Bilevel PAP, BiPAP, or …
Explained: The voluntary Philips Respironics sleep and
In June 2021, Philips initiated a voluntary recall notification / field safety notice for certain CPAP and BiPAP sleep therapy devices and mechanical ventilators to address potential health risks …
Voluntary Recall Information - Philips
2022年12月14日 · While affected devices contained a polyester-based polyurethane (PE-PUR) sound abatement foam component, the sound abatement foam in new and recertified CPAP, …
Explainer on foam used in DreamStation 2 and other devices | Philips
Explained: Silicone sound abatement foam used in DreamStation 2 and the sleep and respiratory care devices remediated as part of the June 2021 Philips Respironics recall* * This is a recall …
Philips provides update on recall notification - News | Philips
2021年6月14日 · Philips issues recall notification* to mitigate potential health risks related to the sound abatement foam component in certain sleep and respiratory care devices
Information for patients and caregivers | Philips
Explained: The voluntary Philips Respironics sleep and respiratory care devices recall* ... No- the replacement device you have received is not affected by the recall/ field safety notice, because …
Voluntary Recall Information - Philips
In June 2021, Philips Respironics issued a voluntary recall notification for specific CPAP and BiPAP devices due to an issue related to the polyester-based polyurethane (PE-PUR) foam …