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Have you been affected by the Philips Respironics PAP Recall?

In June 2021, Philips Respironics recalled a large number of CPAP and other positive airway pressure medical devices over concerns about potential health risks. Now researchers are speaking with patients from across Canada who have been affected to assess how the recall was...
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What is the impact of the Philips Respironics PAP Recall?

In June 2021, Philips Respironics recalled a large number of CPAP and other positive airway pressure medical devices over concerns about potential health risks. Now researchers are speaking with regulators, funders, and policymakers from across Canada who have been impacted to...
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Have your patients been affected by the Philips Respironics PAP Recall?

In June 2021, Philips Respironics recalled a large number of CPAP and other positive airway pressure medical devices over concerns about potential health risks. Now researchers are speaking with healthcare providers from across Canada whose patients have been affected to assess...
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Certain Philips Respironics Masks for BiPAP, CPAP Machines Recalled Due to Safety Issue with Magnets That May Affect Certain Medical Devices

Please review the Links below for information regarding this issue: FDA 2022-09-06 Certain Philips Respironics Masks for BiPAP, CPAP Machines Recalled Due to Safety Issue with Magnets That May Affect Certain Medical Devices | FDA Health Canada  2022-09-26 Magnets in certain...
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Health Canada Advisory Update – Philips Respironics CPAP and BiLevel PAP machines and mechanical ventilators

  UPDATE: Philips Respironics recalls several models of CPAP and BiLevel PAP machines and mechanical ventilators
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SAFETY NOTIFICATION – Potential Risks Associated With The Use of Ozone and Ultraviolet (UV) Light Products

Please see below for important safety information regarding potential risks associated with the use of ozone and ultraviolet (UV) light products to clean CPAP machines and accessories FDA Potential Risks Associated With The Use of Ozone and Ultraviolet (UV) Light Products for...
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MESSAGE FOR VEP CLIENTS USING THE PHILIPS TRILOGY 200 AND BIPAP A40

We have recently learned that Philips Respironics issued a voluntary recall and safety notification for specific ventilator devices due to potential health risks relating to the sound abatement foam used in the devices –...
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URGENT MESSAGE FOR VEP CLIENTS USING THE PHILIPS TRILOGY 200 AND BIPAP A40

On June 14, 2021 Philips Respironics issued a recall on a number of respiratory products including the Trilogy 200 and the BiPAP A40 unit. The recall was issued to mitigate the potential health risks related to the sound absorbing foam. It is recommended that users of the Trilogy...
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A virtual care innovation for home mechanical ventilation

A virtual care innovation for home mechanical ventilation – Canadian Medical Association Journal (CMAJ) Vol. 193, Issue 17 26 Apr 2021 Soins virtuels innovants pour la ventilation mécanique à domicile | CMAJ
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COVID-19 Public Resources Translated in Different Languages

Click here – COVID-19 Public Resources Translated in Different Languages from Public Health Ontario
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