Allura and Azurion Systems recall in Canada: performance issue
In plain language
This recall involves Philips Allura and Azurion Systems sold in Canada. They are being recalled because a component in the uninterruptible power supply (UPS) may fail, causing the system to shut down. This could delay or stop medical procedures, potentially leading to serious health outcomes, including death. Healthcare providers should contact the manufacturer for more information.
What to do
- Contact the manufacturer if you require additional information.
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Affected products
Allura Xper FD20
Model: 722028
Lot: 1039, 1572, 231, 663, 758, 763, 878, 942
Allura Xper FD20 OR Table
Model: 722035
Lot: 111, 128
Azurion 7 B12
Model: 722 067
Lot: 128, 151
Azurion 7 B20
Model: 722 068
Lot: 265, 275
Allura Xper FD10
Model: 722026
Lot: More than 10 numbers, contact manufacturer.
Azurion 7 M12
Model: 722 078, 722 223
Lot: More than 10 numbers, contact manufacturer.
Azurion 7 M20
Model: 722 079, 722 224
Lot: More than 10 numbers, contact manufacturer.
Why this matters
Delay or termination of medical procedures, potentially leading to serious adverse health outcomes, including death.
Do I have this product?
This recall only applies to specific products. Follow the steps below to check.
- 1
Check the product name
Make sure your product name matches one of the affected products listed above.
- 2
Check the lot number
Lot numbers identify specific production batches.
Affected lots: 1039, 111, 128, 151, 1572, 231, 265, 275, 663, 758, 763, 878, 942, More than 10 numbers, contact manufacturer.
- 3
Check the model number
Model numbers are typically on the product label or packaging.
Affected models: 722 067, 722 068, 722 078, 722 079, 722 223, 722 224, 722026, 722028, 722035
If your product matches one or more of the details above, it may be affected by this recall.
If your product does not match these details, it is not affected by this recall.
When in doubt, always check the official notice.
Frequently Asked Questions
Why was this product recalled?
Delay or termination of medical procedures, potentially leading to serious adverse health outcomes, including death.
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. Delay or termination of medical procedures, potentially leading to serious adverse health outcomes, including death.
When was this product recalled?
This product was recalled on August 15, 2025.
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 and Azurion Systems sold in Canada. They are being recalled because a component in the uninterruptible power supply (UPS) may fail, causing the system to shut down. This could delay or stop medical procedures, potentially leading to serious health outcomes, including death. Healthcare providers should contact the manufacturer for more information.