Philips medical systems recall in Canada: Performance issues
In plain language
This recall involves Philips Allura XPER, Allura Centron, and Azurion Systems sold in Canada. They are being recalled because of performance issues with certain components that may lead to loss of system functionality. Contact the manufacturer for more information.
What to do
- Contact the manufacturer if you require additional information.
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Affected products
Specific affected products are listed in the official notice.
Why this matters
Performance issues
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?
Performance issues
What should consumers do?
Contact the manufacturer if you require additional information.
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. Performance issues
When was this product recalled?
This product was recalled on January 19, 2024.
Is the PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. brand affected by this recall?
Yes, PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. products are affected by this recall. This recall involves Philips Allura XPER, Allura Centron, and Azurion Systems sold in Canada. They are being recalled because of performance issues with certain components that may lead to loss of system functionality. Contact the manufacturer for more information.