On June 14, 2021, medical device manufacturer Philips Respironics™ issued a Field Safety Notice regarding the recall of respiratory and ventilator devices due to the health risks associated with their use. Full details of the recall are available on the Philips Respironics™ website.
Please see full list of affected models below:
Continuous Ventilator, Minimal Ventilatory Support, Facility use
- E30
Continuous Ventilator, Non life supporting – BiPAP
- DreamStation ASV
- DreamStation ST, AVAPS
- SystemOne ASV4
- C-Series ASV
- C-series S/T and AVAPS
- OmniLab Advanced +
Non-continuous ventilator
- CPAP
- SystemOne (Q-series)
- DreamStation
- DreamStation Go
- Dorma 400
- Dorma 500
- REMstar SE Auto
Continuous Ventilator
- Trilogy 100
- Trilogy 200
- Garbin Plus, Aeris, LifeVent
Continuous Ventilator, Minimum Ventilatory Support, Facility Use
- A-series BiPAP Hybrid A30
- A-series BiPAP V30 Auto
Continuous Ventilator, Non-life Supporting
- A-series BiPAP A40
- A-series BiPAP A30
The recall does not impact any other devices distributed by Respiratory Homecare Solutions Canada Inc., including the ResMed™ devices.