Continuous Positive Airway Pressure (CPAP), Bi-Level Positive Airway Pressure (BiPAP), and Mechanical Ventilators (2021-06-14)
In plain language
This recall involves Philips Respironics CPAP, BiPAP, and mechanical ventilators sold in Canada. They are being recalled because the sound abatement foam may degrade, potentially releasing particles and chemicals into the device's air pathway. Stop using the product and follow the return/repair steps in the official notice.
What to do
- Stop using the product immediately.
- Contact Philips Respironics for further instructions.
- Consult your healthcare provider for alternative treatment options.
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Affected products
Specific affected products are listed in the official notice.
Why this matters
Chemical exposure and inhalation of foam particles
Do I have this product?
This recall applies to specific products. Details are listed in the official notice.
Frequently Asked Questions
Why was this product recalled?
Chemical exposure and inhalation of foam particles
What should consumers do?
Stop using the product immediately. Contact Philips Respironics for further instructions. Consult your healthcare provider for alternative treatment options.
Where was the product sold?
This product was sold in Canada. For specific retailers or distribution areas, please check the official recall notice linked on this page.
Is there a health risk?
Yes, there may be a health risk. Chemical exposure and inhalation of foam particles
When was this product recalled?
This product was recalled on June 23, 2021.
Is the Philips Respironics brand affected by this recall?
Yes, Philips Respironics products are affected by this recall. This recall involves Philips Respironics CPAP, BiPAP, and mechanical ventilators sold in Canada. They are being recalled because the sound abatement foam may degrade, potentially releasing particles and chemicals into the device's air pathway. Stop using the product and follow the return/repair steps in the official notice.