Azurion and Allura Systems recall in Canada: finger entrapment risk
In plain language
This recall involves Azurion and Allura Systems medical devices sold in Canada. They are being recalled because a finger can get entrapped during manual repositioning of the patient tabletop, possibly resulting in injury. Stop using the product and contact the manufacturer for more information.
What to do
- Stop using the product immediately.
- Contact the manufacturer if you require additional information.
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Affected products
Allura Xper FD10
Model: 001443
Allura Xper FD20 OR Table (Product Of AlluraClarity Family)
Model: 722035
Allura Xper FD20/10 (Product Of AlluraClarity Family)
Model: 722029
Allura Xper FD20/15
Model: 722058
Azurion 7 M20
Model: 722 224 722 079 722234
Azurion 3 M12
Model: 722 063 722 221
Azurion 3 M15
Model: 722 064 722 222
Azurion 7 B12
Model: 722 067 722235 722 225
Allura Xper FD10/10 (Product Of AlluraClarity Family)
Model: 722027
Azurion 7 M12
Model: 722233 722 223 722 078
Allura Xper FD10 (Product Of AlluraClarity Family)
Model: 722026
Allura Xper FD20 (Product Of AlluraClarity Family)
Model: 722028
Allura Xper FD20/20 (Product Of AlluraClarity Family)
Model: 722038
Azurion 7 B20
Model: 722 226 722236 722 068
Azurion 5 M12
Model: 722 227 722231
Azurion 5 M20
Model: 722 228 722232
Why this matters
Finger entrapment 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 model number
Model numbers are typically on the product label or packaging.
Affected models: 001443, 722 063 722 221, 722 064 722 222, 722 067 722235 722 225, 722 224 722 079 722234, 722 226 722236 722 068, 722 227 722231, 722 228 722232, 722026, 722027, 722028, 722029, 722035, 722038, 722058, 722233 722 223 722 078
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?
Finger entrapment risk
What should consumers do?
Stop using the product immediately. 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. Finger entrapment risk
When was this product recalled?
This product was recalled on January 30, 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 Azurion and Allura Systems medical devices sold in Canada. They are being recalled because a finger can get entrapped during manual repositioning of the patient tabletop, possibly resulting in injury. Stop using the product and contact the manufacturer for more information.