Medical Device Recall Information - Philips Respironics Sleep …
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
2023年6月29日 · Please log-in to the Patient Portal for device specific instructions on how Philips Respironics can obtain your prescription and fulfill your replacement device. Depending on your specific situation, you may be eligible to select an Auto-adjusting CPAP replacement device.
Philips Respironics Sleep and Respiratory Care devices | Philips
2023年9月27日 · Registration for affected CPAP and BiPAP devices in the US and Canada ends at 11:59 p.m. EST, December 31, 2024. Globally, we have remediated 99% of actionable* sleep therapy device registrations to date.
Sleep and respiratory care update | Philips
Register affected devices on the recall notification (U.S. only) / field safety notice (International Markets) website, www.philips.com/SRC-update.
Remediation progress update - Philips
2024年11月25日 · Globally, we have remediated 99% of actionable* sleep therapy device registrations to date. Continuing to remediate new and existing registrations remains our priority. We will make multiple attempts to ensure we have the information needed to place an order, and will provide responding patients with remediation options.
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...
Sleep respiratory recall | Philips
Register affected devices on the recall notification (U.S. only) / field safety notice (International Markets), www.philips.com/SRC-update. The website provides current information on the status of the recall notification (U.S. only) / field safety notice (International Markets) and how to receive permanent corrective action to address the two ...
Testing results for affected devices - Philips
2023年5月16日 · In June 2021, after discovering potential health risks related to the polyester-based polyurethane (PE-PUR) sound abatement foam in certain CPAP, BiPAP and Mechanical Ventilator devices, Philips Respironics issued a voluntary recall notification.
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.