Philips Respironics recalls several models of CPAP and BiLevel PAP machines and mechanical ventilators
Recalled Product
Philips Respironics Continuous Positive Airway Pressure (CPAP) machines, BiLevel Positive Airway Pressure (BiLevel PAP) machines and mechanical ventilators
Hazard / Issue
Performance
Issued by
Communications and Public Affairs Branch
⚠️ What You Should Do
Register your device on the Philips recall website or call its recall hotline at 1-877-907-7508. Philips has established a registration process where you can look up your device serial number and begin a claim if your unit is affected.If you have an affected product talk to your physician, or medical device provider first before stopping or changing how you use your product, as the benefits of using these devices may outweigh the risks for many users.Be sure to clean your device only according to the manufacturer’s Instructions for Use, as the use of non-validated cleaning methods (e.g. ozone) could contribute to potential foam degradation.Do not attempt to remove or replace the foam yourself.Report any health product-related side effects or complaints to Health Canada.
Were you affected by this recall?
If you were harmed by a recalled product, you may have legal options. Consider speaking with a consumer protection lawyer in your province.
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