Allura Xper Systems recall in Canada: device compatibility issue
In plain language
This recall involves Allura Xper Systems medical devices sold in Canada. They are being recalled because a missing component may cause the device to fail. 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 FD20/20 (Product Of Alluraclarity Family)
Model: 722038
Lot: Not applicable.
Allura Xper FD20 OR Table (Product Of Alluraclarity Family)
Model: 722058
Lot: Not applicable.
Allura Xper FD10
Model: 001443
Lot: 608
Allura Xper FD10/10 (Product Of Alluraclarity Family)
Model: 722027
Lot: Not applicable.
Allura Xper FD20/10 (Product Of Alluraclarity Family)
Model: 722029
Lot: Not applicable.
Allura Xper FD10 (Product Of Alluraclarity Family)
Model: 722026
Lot: 1115
Allura Xper FD20 (Product Of Alluraclarity Family)
Model: 722028
Lot: 1094, 1681, 2282
Why this matters
Device compatibility 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: 1094, 1115, 1681, 2282, 608, Not applicable.
- 3
Check the model number
Model numbers are typically on the product label or packaging.
Affected models: 001443, 722026, 722027, 722028, 722029, 722038, 722058
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?
Device compatibility 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. Device compatibility issue
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 Allura Xper Systems medical devices sold in Canada. They are being recalled because a missing component may cause the device to fail. Contact the manufacturer for more information.