Does Your Device Qualify for the Recall?

In June 2021, Philips recalled millions of its CPAP and BiPAP machines as well as several ventilator devices that were manufactured between 2009 and April 26, 2021.  The recall was caused by potential health risks associated with exposure to the degraded sound abatement foam particles and chemical emissions from the foam material. 

The Philips BiPAP and CPAP machines and ventilators that are affected by the recall include: 

  • E30 (Emergency Use Authorization) 
  • DreamStation ASV 
  • DreamStation ST, AVAPS 
  • SystemOne ASV4 
  • C Series ASV, S/T, AVAPS 
  • OmniLab Advanced Plus In-Lab Titration Device 
  • SystemOne (Q series) 
  • DreamStation CPAP, Auto CPAP, BiPAP 
  • DreamStation GO CPAP, APAP 
  • Dorma 400, 500 CPAP 
  • REMStar SE Auto CPAP 
  • Trilogy 100 Ventilator 
  • Trilogy 200 Ventilator 
  • Garbin Plus, Aeris, LifeVent Ventilator 
  • A-Series BiPAP V30, A30 & A40 Ventilators 
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