Tag: BiPAP

Product & Vendor Updates Drug Recalls & Safety Notices Patient Health & Care Sleep Devices & Equipment

Certain Philips Respironics Masks Recalled Due to Safety Issue

The U.S. Food and Drug Administration (FDA) is alerting patients, caregivers, and health care providers that Philips Respironics (Philips) recalled certain masks used with bilevel positive airway pressure (also known as Bilevel PAP, BiPAP, or BPAP) machines and continuous positive airway pressure (CPAP) machines due to a serious safety concern. The […]

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藥物召回與安全公告

CPAP Class Action Lawsuit Filed Against Philips

The national plaintiffs’ law firm Berger Montague has filed a class action lawsuit against Dutch medical equipment company Philips to protect consumers harmed by Philips’ recalled sleep apnea machines, including CPAP and BiPAP machines, and ventilators, which may increase users’ risk of cancer and pulmonary fibrosis, and cause other injuries […]

philips
藥物召回與安全公告

Philips Voluntarily Recalls Millions of PAPs and Ventilators

Following the company update on 四月 26, 2021, Royal Philips has provided an update on the recall notification* for specific Philips Bi-Level Positive Airway Pressure (Bi-Level PAP), Continuous Positive Airway Pressure (CPAP), and mechanical ventilator devices to address identified potential health risks related to the polyester-based polyurethane (PE-PUR) sound abatement foam component […]