Medical Device Recall Information - Philips Respironics Sleep and ...
Registration for affected CPAP and BiPAP devices in the US and Canada ends at 11:59 p.m. EST, December 31, 2024. An update on our progress. Globally, we have remediated 99% of actionable* sleep therapy device registrations to date.
Contact and support for Philips Respironics voluntary recall
Registration for affected CPAP and BiPAP devices in the US and Canada ends at 11:59 p.m. EST, December 31, 2024. Contact and support options for patients impacted by the June 2021 voluntary recall of certain CPAP, BiPAP and mechanical ventilators related to PE-PUR sound abatement foam.
Voluntary Recall Information - Philips
3 天之前 · Philips Respironics will not accept new registrations for affected CPAP and BiPAP devices in the US after December 31, 2024. Please check the US Patient Portal to take any necessary steps in receiving your replacement device as soon as possible. The US Patient Portal will remain open until June 30, 2025.
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 continuous positive...
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 BPAP) machines,...
Philips Respironics Sleep and Respiratory Care devices | Philips
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).
Recommendations for Recalled Philips Ventilators, BiPAP …
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 continuous positive airway...
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 related to the polyester-based polyurethane (PE-PUR) sound abatement foam in these devices.
Recalled Philips sleep apnea machines linked to 500 deaths: FDA - USA TODAY
2024年2月2日 · The U.S. Food and Drug Administration (FDA) has issued an update to a recall affecting millions of Philips sleep apnea machines, saying that they may be linked to at least 561 reported deaths.
Philips Respironics Sleep and Respiratory Care devices | Philips
Please continue to follow the field safety notice instructions you have received for affected Philips Respironics Sleep & Respiratory Care devices. The latest information regarding this action can be found at our publicly available web site: www.philips.com/src-update
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