Are You Eligible to File a Claim for Injuries Related to Camp Lejeune?
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.