http://lw.hmpgloballearningnetwork.com/site/pcn/videos/new-national-988-mental-health-crisis-response-hotline-highlighted-need 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 …
CPAP Recall Over Potential Cancer Risks Leaves Millions …
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. WebbRecall of CPAP, BiPAP and Ventilators relating to the PE-PUR sound abatement foam. I have not yet registered my affected device / need to change my registration information. … cpdm sharepoint
Informations Sur Le Rappel de Philips Respironics - VitalAire
Webb7 apr. 2024 · Devices Recalled in the U.S.: 1,088; Date Initiated by Firm: February 10, 2024; Note: This recall is for certain reworked DreamStations that were also recalled in June 2024. Device Use. Philips Respironics (Philips) DreamStation devices help people with breathing conditions keep breathing at a regular rhythm. Webb9 feb. 2024 · Read more in the safety communication for Certain Reworked Philips Respironics Trilogy 100/200 Ventilators Recalled Due to Potential for Silicone Foam … 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 … disney world passholder sign in