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In June 2021, after discovering a potential health risk related to a part in certain CPAP, BiPAP and Mechanical Ventilator devices, Philips issued a voluntary Field Safety Notice (outside U.S.) / voluntary recall notification (U.S. only).
Voluntary Recall Information. Philips Respironics Sleep and Respiratory Care devices. Registration for affected CPAP and BiPAP devices in the US and Canada ends at 11:59 p.m. EST, December 31, 2024. Register now. Learn more.
Philips Respironics acted to protect patient safety by initiating and executing a voluntary recall* of significant scale in June 2021. Philips regrets any distress and concern this recall* has caused patients, their families and care providers.
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...
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...
Philips Respironics is voluntarily recalling the below devices due to two (2) issues related to the polyester-based polyurethane (PE-PUR) sound abatement foam used in Philips Continuous and Non- Continuous Ventilators: 1) PE-PUR foam may degrade into particles which may enter the device’s the air
Voluntary Recall Information. Philips Respironics Sleep and Respiratory Care devices. Registration for affected CPAP and BiPAP devices in the US and Canada ends at 11:59 p.m. EST, December 31, 2024. Important information for clinicians. Sleep Therapy information.
For more information on the recall notification, as well as instructions for customers, users and physicians, affected parties may contact their local Philips representative or visit www.philips.com/SRC-update. Call 877-907-7508 if you cannot visit the website or do not have internet access.
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).
Latest updates. Explained: The voluntary Philips Respironics sleep and respiratory care devices recall* * This is a voluntary recall notification in the US and field safety notice in other countries. Learn more. Explained: The Philips Respironics Consent Decree. April 4, 2024. Learn more. All news and updates.