Official recall record

Allura Xper and Azurion Systems

What the authority reported

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.

What to do

Follow the instructions in the official notice — recall remedies (refund, repair, replacement, or disposal) are defined by the issuing authority and the responsible business, and they differ per recall. Do not rely on summaries, including this one.

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