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Respiratory therapy – St Clair County Community College
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Koninklijke Philips N : Royal Philips - Philips issues recall notification to mitigate potential health risks related to the sound abatement foam component in certain sleep and respiratory care devices
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June 14, 2021
Philips is initiating a voluntary recall notification to ensure patient safety in consultation with regulatory agencies
Corrective actions include the deployment of updated instructions for use and a repair and replacement program for affected devices
Philips aims to address all affected devices within the scope of this correction as expeditiously as possible
Amsterdam, the Netherlands – Following the company
update on April 26, 2021,
Royal Philips (NYSE: PHG; AEX: PHIA) today provides an update on the recall notification for specific Philips Bi-Level Positive Airway Pressure (Bi-Level PAP), Continuous Positive Airway Pressure (CPAP), and mechanical ventilator devices to address identified potential health risks related to the polyester-based polyurethane (PE-PUR) sound abatement foam component in these devices. The majority of the affected devices within the advised 5-year service life are in the first-generation DreamStation product family.
Philips Recalls Certain Sleep And Respiratory Care Devices
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