« All FAQ About CPAP Lawsuits

What Products Were Involved in the Phillips Breathing Machine Recall?

Following the emergence of a range of health complaints, MedTech company Phillips has issued a recall for several Respironics ventilators, including CPAP machines, bi-level positive airway pressure (BiPAP) machines, and mechanical ventilators.

The recall list includes the following CPAP and BiPAP machines:

Continuous Ventilator, Minimum Ventilatory Support, Facility Use

  • E30 (emergency use authorization)

Continuous Ventilator, Non-Life Supporting

  • DreamStation ASV
  • DreamStation ST, AVAPS
  • SystemOne ASV4
  • C-Series ASV
  • C-Series S/T and AVAPS
  • OmniLab Advanced+

Noncontinuous Ventilator

  • SystemOne (Q-Series)
  • DreamStation
  • DreamStation Go
  • Dorma 400
  • Dorma 500
  • REMstar SE Auto

The recall also specifies the following ventilators:

Continuous Ventilator

  • Trilogy 100
  • Trilogy 200
  • Garbin Plus, Aeris, LiveVent

Continuous Ventilator, Minimum Ventilatory Support, Facility Use

  • A-Series BiPAP Hybrid A30 (not marketed in the U.S.)
  • A-Series BiPAP V30 Auto

Continuous Ventilator, Non-life Supporting

  • A-Series BiPAP A40
  • A-Series BiPAP A30

If you use or have used any of the machines cited on the recall list, you should speak to your doctor immediately. Then, contact The Ruth Law Team to find out if you might be eligible to join a class-action lawsuit against Phillips.

Related Questions:

What are the symptoms related to the CPAP lawsuit?

Notification of the Phillips Respironics defects was first released in April of 2021, followed by the recall in June.  The company is estimating that as many as 3-4 million devices sold before April of 2021, the majority of which are DreamStation models, may be subject to flaws that carry a significant risk of lung injury,… read more?