Philips Azurion and Allura Systems recall in Canada: performance issue
In plain language
This recall involves Philips Azurion and Allura Systems medical devices used in healthcare settings in Canada. They are being recalled because bolts supporting the flexmove carriage may become loose or break, and cracks may appear. Healthcare professionals should contact the manufacturer for additional information.
What to do
- Contact the manufacturer if you require additional information.
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Affected products
Allura Xper FD10 (Product Of AlluraClarity Family)
Model: 722 224 722 079
Lot: Not applicable.
Allura Xper FD10
Model: 722026
Lot: Not applicable.
Allura Xper FD20 Or Table (Part Of AlluraClarity Family)
Model: 001443
Lot: Not applicable.
Allura Xper FD20 (Product Of AlluraClarity Family)
Model: 722035
Lot: Not applicable.
Allura Xper FD20
Model: 722028
Lot: Not applicable.
Why this matters
Performance issue
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: Not applicable.
- 3
Check the model number
Model numbers are typically on the product label or packaging.
Affected models: 001443, 722 224 722 079, 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?
Performance issue
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 issue
When was this product recalled?
This product was recalled on June 22, 2023.
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 and Allura Systems medical devices used in healthcare settings in Canada. They are being recalled because bolts supporting the flexmove carriage may become loose or break, and cracks may appear. Healthcare professionals should contact the manufacturer for additional information.