Philips Allura Xper recall in Canada: Performance issues
In plain language
This recall involves Philips Allura Xper medical devices sold in Canada. It's being recalled because potential safety issues could cause parts of the system to not function as expected. Healthcare professionals should 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.
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?
This recall involves Philips Allura Xper medical devices sold in Canada. It's being recalled because potential safety issues could cause parts of the system to not function as expected. Healthcare professionals should contact the manufacturer for more information.
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?
A potential safety risk has been identified with this product. Stop using it immediately and follow the instructions in the official recall notice.
When was this product recalled?
This product was recalled on November 29, 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 medical devices sold in Canada. It's being recalled because potential safety issues could cause parts of the system to not function as expected. Healthcare professionals should contact the manufacturer for more information.