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Philips Respironics is a serious recall, FDA officials say - CBS News
WebbAlthough we are not responsible for the Philips Respironics recall, we want to support our patients through this difficult time. We have been working diligently with Philips Respironics to ensure our patients receive continual updates. As we learn more, we will update our website here. Or, contact us to learn more. Call Us at (800) 673-1220 Webbför 9 timmar sedan · Philips ( NYSE: PHG) clarified its product recall for respiratory devices on Friday after the FDA warned that the number of replaced or repaired products is considerably less than the company's ... open foundary
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WebbA PHILIPS MEDICAL informa que está recolhendo voluntariamente os seus aparelhos de sono e respiração fabricados até 26 de abril de 2024, de acordo com os seguintes modelos: Aparelhos de CPAP e BiPAP. Aparelhos de Ventilação. Webb14 juni 2024 · June 14, 2024. Philips is initiating a voluntary recall notification* to ensure patient safety in consultation with regulatory agencies; Corrective actions include the deployment of updated ... Webb14 juni 2024 · The updated recall notification advises patients using bi-level PAP and CPAP devices to consult with their physician on a suitable treatment plan. Patients, physicians and durable medical equipment (DME) suppliers can call Philips at 877-907-7508 for additional support. Repair and Replacement open for you