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MEDICAL RECALL 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.  Please see below for current information from the VEP.

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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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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