Inhaling the foam can cause "serious injury which can be life-threatening," Philips wrote in its company recall at the time. The company tried to fix some of the machines, but the repaired ones have also been recalled, according to the U.S. Food and Drug Administration. "The FDA has...
Philips CPAP Recall Lawsuit Philips Respironics has recalled certain mechanical ventilators, BiPAP, and CPAP machines due to potential health risks, including cancer. If you’ve used a Philips sleep apnea machine and experienced injuries or illnesses as a result, you may be eligible to receive ...
If you, or someone you love, have been using a Philips Respironics machine included in the updated recall, speak with your doctors immediately. It is not recommended to stop using the machine until health care providers can determine an alternative solution. You may also be eligible to pursue ...
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BiPAP A40 Pro Basic Setup & Return Instructions The enclosed BiPAP A40 Pro device is provided to you as a replacement for your current A-Series BiPAP device. This document provides basic instructions for setting up your replacement device and for returning your current device.To ensure proper ...
illions of Americans’ bedtime routine includes wearing a mask attached to a respiratory machine that pushes air into their lungs, supporting their breathing during sleep. These airway pressure machines, known as CPAP or BiPAP depending on their design, are sophisticated medical devices that have bee...
TheU.S. Food and Drug Administration (FDA)classified this recall asClass I– the most serious – because using the affected Philips CPAP/BiPAP and ventilator devices may cause serious injuries or death. This recall affects more than 15 million breathing devices. Note that the Respironics M-Serie...
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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. Learn More > Sleep and Respiratory Care Patients and Caregivers DMEs and Distributors Clinicians Recall ...