Azurion 3 and 7 recall in Canada: Medical device performance issues
In plain language
This recall involves Azurion 3 and 7 medical devices sold in Canada. They are being recalled because of software issues that may affect system performance. 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
Azurion 3
Model: 722 063, 722 064
Lot: M12, M15
Azurion 7
Model: 722 067, 722 068, 722 078, 722 079
Lot: B12, B20, M12, M20
Why this matters
Medical device performance issues
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: B12, B20, M12, M15, M20
- 3
Check the model number
Model numbers are typically on the product label or packaging.
Affected models: 722 063, 722 064, 722 067, 722 068, 722 078, 722 079
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?
Medical device 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. Medical device performance issues
When was this product recalled?
This product was recalled on August 14, 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 Azurion 3 and 7 medical devices sold in Canada. They are being recalled because of software issues that may affect system performance. Healthcare professionals should contact the manufacturer for more information.