FDA says 561 deaths tied to recalled Philips sleep apnea machines::Update from the Food and Drug Agency comes days after Philips said it would stop selling the devices in the U.S.
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More info is needed. Here ya go folks:
Philips recalled the following devices made between 2009 and April 26, 2021:
A-Series BiPAP A30 A-Series BiPAP A40 (ventilator) A-Series BiPAP Hybrid A30 A-Series BiPAP V30 Auto (ventilator) C-Series ASV (ventilator) C-Series S/T and AVAPS DreamStation DreamStation ASV DreamStation Go DreamStation ST, AVAPS Dorma 400 Dorma 500 E30 Garbin Plus, Aeris, LifeVent (ventilator) OmniLab Advanced+ REMstar SE Auto SystemOne ASV4 SystemOne (Q-Series) Trilogy 100 (ventilator) Trilogy 200 (ventilator)
