Philips Medical Systems Nederland B.V. recalled the Allura Xper FD20/20 medical imaging system on December 15, 2025, due to a potential electrical hazard. The recall affects eight units globally, including those distributed in the United States and several other countries. A missing drip tray can lead to coolant contacting electrical components, posing a risk of electrical short circuits and total
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 recalled product is the Allura Xper FD20/20, Model Number 722038. It was distributed worldwide, including the US, since its initial rollout. Eight units are affected in this recall.
If the drip tray beneath the cooling unit is not installed, coolant may contact electrical components. This can lead to electrical short circuits that trigger system fuses, potentially causing a system shutdown.
There are no reported injuries or incidents associated with this recall. The recall is proactive to prevent potential hazards.
Stop using the Allura Xper FD20/20 immediately. Follow the manufacturer's recall instructions and contact Philips Medical Systems Nederland B.V. or your healthcare provider for further instructions.
For more information, contact Philips Medical Systems Nederland B.V. at the provided recall link: https://www.accessdata.fda.gov/scripts/enforcement/enforce_rpt-Product-Tabs.cfm?recall_number=Z-1077-2026.
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