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 continuous positive...

Registration for affected CPAP and BiPAP devices in the US and Canada closed on December 31, 2024. The Patient Portal will remain open for registered US patients until June 30, 2025. An update on our progress. Globally, we have remediated 99% of actionable* sleep therapy device registrations to date.

2024年2月2日 · Philips has agreed to stop selling sleep apnea machines in the U.S. and existing devices manufactured between 2009 and April 2021 are subject to recall, as they may pose a serious injury risk...

2023年9月28日 · After receiving thousands of complaints, Philips announced a recall of about 20 models of ventilators and CPAP (continuous positive airway pressure) and BiPAP (bi-level positive airway...

Philips is recalling certain reworked Philips DreamStations because some devices were assigned incorrect or duplicate serial numbers during initial programming. This duplication can cause...

In April 2021, Philips first notified the FDA of their intention to conduct a field action due to concerns pertaining to foam breakdown in certain ventilators, BiPAP machines, and CPAP...

2024年2月4日 · The FDA said that since April 2021 it has received more than 116,000 medical device reports of foam breaking down in Philips CPAP (continuous positive airway pressure) machines and BiPAP...

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.

On June 14, 2021, Philips initiated a voluntary U.S. recall (and an international field safety notice) for specific Philips Respironics models of continuous positive airway pressure (CPAP), bilevel positive airway pressure (BPAP), and mechanical ventilator devices.

Philips has updated the US recall notification to align with the FDA’s recommendation in connection with these recalls and provide broader guidance on use. For patients using BiLevel PAP and CPAP devices, consult with your physician on a suitable treatment plan.