Philips Medical Systems Nederland B.V. recalled 56 Allura Xper FD10 systems on December 15, 2025. The recall stems from a potential electrical hazard where coolant may contact electrical components, risking short-circuits. Healthcare providers must cease use immediately and follow provided instructions.
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 Allura Xper FD10 is a medical imaging system used in healthcare settings for diagnostic procedures. It is designed to provide high-quality imaging for various medical applications.
The absence of a properly installed drip tray can lead to coolant leaks that may contact electrical components. This can cause electrical short-circuits, posing a risk of system failure.
This recall is not part of a broader industry pattern.
Healthcare providers must stop using the affected systems, which may disrupt medical services temporarily.
The model number and serial numbers can typically be found on the back or bottom of the device.
Expect a timeline of 4-6 weeks for processing refunds or replacements after returning the device.
Keep records of your purchase, any correspondence with Philips, and photos of the device as evidence.
The recall affects Allura Xper FD10, Model Number 722010. It was distributed worldwide, including the US and several international markets. The systems were sold under various identifiers, including UDI-DI 00884838059030.
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