WebbRESPIRONICS RECALL UPDATE – DECEMBER 2, 2024 URGENT: Medical Device RecallPhilips RespironicsCPAP and Bi-Level PAP Devices To our valued customers: Since we announced a recall of certain products in our Sleep & Respiratory Care portfolio on June 14, 2024, Philips Respironics has been working in close partnership with competent. Webb1 mars 2024 · Philips Respironics is recalling the following devices due to issues with the polyester-based polyurethane foam (PE-PUR), sound abatement foam, used in Philips Continuous Ventilators and NonContinuous Ventilators. The PE-PUR foam could degrade into small particles that can enter the device's airway and be inhaled or inhaled by users.
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Webb8 juli 2024 · US-FDA inspection of Philips Respironics Inc. ... You can do this via the Philips Electronics Australia Ltd support hotline on 1800 009 579. ... Philips recall action for … Webb14 juni 2024 · Philips issues recall notification* to mitigate potential health risks related to the sound abatement foam component in certain sleep and respiratory care devices … green outdoor extension cords
A recall of Philips respiratory devices has left users stranded
WebbAbout Philips Respironics As a global leader in the sleep and respiratory markets, we're passionate about providing solutions that lead to healthier patients, practices, and … WebbRead the Field Safety Notice for ventilators (FSN 2024-05-A) (111.0KB) Check the affected device list Register your device (s) Questions and answers Support line 0800 249 4578 … Webb22 apr. 2024 · Philips Respironics has identified that there is a possibility that affected ventilator units may cease to operate, potentially without setting off an audible/visual … f. lynne bachleda