Philips Azurion, Allura Xper and Eleva Systems
In plain language
This recall involves Philips Azurion, Allura Xper, and Eleva Systems medical devices used in healthcare settings in Canada. They are being recalled because a cable carrier can detach and strike individuals, posing a head injury risk. Healthcare facilities should contact the manufacturer for more information.
What to do
- Contact the manufacturer for additional information.
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Affected products
Specific affected products are listed in the official notice.
Why this matters
Head injury risk
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?
Head injury risk
What should consumers do?
Contact the manufacturer for 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. Head injury risk
When was this product recalled?
This product was recalled on September 9, 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 Azurion, Allura Xper, and Eleva Systems medical devices used in healthcare settings in Canada. They are being recalled because a cable carrier can detach and strike individuals, posing a head injury risk. Healthcare facilities should contact the manufacturer for more information.