Philips Allura and Azurion recall in Canada: falling part risk
In plain language
This recall involves Philips Allura and Azurion medical devices sold in Canada. They are being recalled because a part could fall and injure patients or staff. Healthcare facilities should contact the manufacturer for more information.
What to do
- Stop using the product immediately.
- Contact the manufacturer for additional information.
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Affected products
Allura Xper Fd10 (Product Of Alluraclarity Family)
Model: 722026
Lot: All lots
Allura Xper Fd20 Or Table (Part Of Alluraclarity Family)
Model: 722035
Lot: All lots
Vitros Chemistry Products System - Eco2 Slides (Carbon Dioxide)
Model: 722 227
Lot: All lots
Integris H5000c Cardiology Imaging System
Model: 722016
Lot: All lots
Azurion 5 M20
Model: 722 228
Lot: All lots
Allura Xper Fd10
Model: 001443
Lot: All lots
Allura Xper Fd20/15
Model: 722058
Lot: All lots
Allura Xper Fd10 Or Table (Product Of Alluraclarity Family)
Model: 722033
Lot: All lots
Allura Xper Fd20 (Product Of Alluraclarity Family)
Model: 722028
Lot: All lots
Allura Xperfd20/20 (Product Of Alluraclarity Family)
Model: 722038
Lot: All lots
Azurion 7 M12
Model: 722 223 722 078
Lot: All lots
Azurion 7 M20
Model: 722 224 722 079
Lot: All lots
Why this matters
Falling object risk
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: All lots
- 3
Check the model number
Model numbers are typically on the product label or packaging.
Affected models: 001443, 722 223 722 078, 722 224 722 079, 722 227, 722 228, 722016, 722026, 722028, 722033, 722035, 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?
Falling object risk
What should consumers do?
Stop using the product immediately. 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. Falling object risk
When was this product recalled?
This product was recalled on November 24, 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 Allura and Azurion medical devices sold in Canada. They are being recalled because a part could fall and injure patients or staff. Healthcare facilities should contact the manufacturer for more information.