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Allura xper and azurion systems
Official notice
17 Mar 2026
Last checked
17 Mar 2026
An official Health Canada notice concerns Allura xper and azurion systems. Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch due to: cable or connector damage (internal and/or external) internal microswitch failure (each foot switch pedal activates two independent microswitches that - when both activated - release X-ray) foot switch connector issues resulting from missing or incorrectly applied strain relief No or intermittent X-ray could potentially result in a delay or abort of procedure. Published 2026-03-17.
What to do now
Contact the manufacturer if you require additional information.
Recall number
81765
Official notice
2026-03-17
The hazard
The hazard
Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch due to: cable or connector damage (internal and/or external) internal microswitch failure (each foot switch pedal activates two independent microswitches that - when both activated - release X-ray) foot switch connector issues resulting from missing or incorrectly applied strain relief No or intermittent X-ray could potentially result in a delay or abort of procedure.
How to check if you're affected
How to check if you're affected
Compare the VIN on your vehicle against the official list. If your VIN is listed, follow the official notice.
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Affected products
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Risk / hazard
Where it was sold
Where it was sold
The source does not list specific retailers. See the official notice for where affected vehicles were sold.
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Affected area 1
Company & contacts
Company & contacts
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Phone
Brand: Philips.
Source & status
Source & status
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Recall details
Recall details
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Documents, notices & source
See the official notice and source documents for full details.
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