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3 cze 2024 · Amid concerns of health problems associated with the sound abatement foam used in their continuous positive airway pressure (CPAP) devices, Philips Respironics issued a voluntary recall on 5.5 million ventilators, BiPAP machines, and …
29 sty 2024 · In 2021, Philips Respironics determined from user reports and initial testing that there were possible risks to users related to the polyester-based polyurethane (PE-PUR) sound abatement foam used in specific CPAP, BiPAP and ventilator devices. Following the issuance of the recall
5 gru 2023 · If you're experiencing an issue with a part on your machine, you may want to check out the PerfectDraft Machine - Warranty & Repairs article. If you have the Original PerfectDraft Machine, you can sometimes purchase spares directly from the manufacturer here.
Voluntary Recall Information. Philips Respironics Sleep and Respiratory Care devices. 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 (outside U.S.) / voluntary recall notification (U.S. only).
6 paź 2023 · Philips makes no representations or warranties of any kind with regard to any third-party websites or the information contained therein. I understand You are about to visit a Philips global content page
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 related to the polyester-based polyurethane (PE-PUR) sound abatement foam in these devices.
5 paź 2023 · In June 2021, Philips Respironics (Philips) recalled certain ventilators, bi-level positive airway pressure (also known as Bilevel PAP, BiPAP, or BPAP) machines, and continuous positive...
