Philips recalled four units of the Allura Xper FD20 OR Table on December 15, 2025, due to a potential electrical hazard. The drip tray installation issues could allow coolant to contact electrical components, risking short-circuits and system shutdowns. Healthcare providers and patients must stop using the device immediately.
Philips has identified that in a limited number of impacted systems the drip tray beneath the cooling unit was not installed under previous field corrections, or evidence of the implementation was not adequately documented. If it is not installed, there is a potential for coolant liquid to contact electrical components. This could lead to electrical short-circuits, which may trigger system fuses and result in system shutdown.
Patients and healthcare providers should stop using this device immediately. Follow the recall instructions provided by the manufacturer. Contact PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. or your healthcare provider for instructions. Notification method: Letter
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The recall affects the Allura Xper FD20 OR Table, Model Number 722023. The recalled units have serial numbers 10, 85, and 125. The product was distributed worldwide, including the US and various countries.
Philips identified that the drip tray beneath the cooling unit may not have been installed correctly. If coolant contacts electrical components, it could cause short-circuits, triggering system fuses and resulting in shutdown.
There have been no reported incidents or injuries associated with this recall. The potential for electrical failure remains a serious concern.
Stop using the Allura Xper FD20 OR Table immediately. Contact Philips Medical Systems for further instructions and follow the recall procedures provided in the notification letter.
For more information, contact Philips Medical Systems Nederland B.V. at the number provided in the recall letter. Visit the FDA website for additional details.
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