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Health Canada Medical devices

Philips Multidiagnost Eleva, Allura Xper and Azurion systems

Issued August 21, 2023
Issue
Philips has become aware of a potential safety issue with the wired and wireless foot switch used with the Philips Multidiagnost Eleva, Allura Xper and Azurion systems, where there is a possibility of unintended radiation. The wired and wireless foot switch are used to control fluoroscopy, exposure and other functions, such as single shot, light control and toggle between x‐ray planes (for bi‐plane systems). A foot switch pedal may get stuck in the active position when the user releases the pedal, resulting in the emission of unintended radiation, because of: • Build‐up of dense or sticky fluids on the foot switch (e.g., blood or contrast fluid), if not properly cleaned. • Use of protective covers that are either the wrong size or incorrectly placed on the foot switch. • Dislodgement of a screw holding the handle of the foot switch, subsequently becoming lodged within the foot switch housing. • An additional screw inadvertently left inside the foot switch housing during manufacturing. Philips has not received any reports of harm resulting from sticking foot switches. Recall Start Date: August 9, 2023
Hazard description
Performance
Product
Product name
Philips Multidiagnost Eleva, Allura Xper and Azurion systems
Reference
ID
RA-74140