![]() ![]() If you have concerns about using your device, please also reach out to your physician with any questions you may have regarding your therapy. Philips has not provided the timing of the availability of potential future product replacement. Welcome to the official Philips page Headquartered in the Netherlands, were a company of approximately 114,000 employees serving people in more than 100 countries. After registration, they will notify you with additional information as it becomes available.Īdvanced Home Medical is in communication with Philips about this recall and we will do our best to provide information to you as it is relayed to us as promptly as possible. If you are in the United States, you will receive a letter by Jfrom Philips about this issue that contains log-in credentials for the registration website. Amsterdam, the Netherlands and Nashville, TN, USA Royal Philips (NYSE: PHG, AEX: PHIA), a global leader in health technology, and Vanderbilt University Medical Center (VUMC. ![]() For information on the Recall Notice, a complete list of impacted products, and potential health risks, visit Using this link, you can begin to register your impacted machine. When questions or service needs arise, you want direct access to trained individuals with the skills and tools to provide you with the right solution fast. On June 14, 2021, Philips Respironics announced a voluntary recall for Continuous and Non-Continuous Ventilators (certain CPAP, BiLevel PAP, and Ventilator Devices) due to related polyester-based polyurethane (PE-PUR) sound abatement foam used in these 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. We want to make you aware of an important development related to certain CPAPs, BiLevel PAPs, and Ventilators (including non-invasive and invasive ventilation) manufactured by Philips Respironics. ![]()
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