Philips Medical Systems Netherlands B.V. recalled 3 Allura Xper FD20/20 OR Tables worldwide, including the US, on 2025-09-03 after detection of degradation in internal components. The recall cites CMOS battery, hard disk drive, and/or power supply unit deterioration. Motorized movements may fail while imaging remains available. The recall is active. Stop using the device following recall guidance.
Systems may not perform as intended due to the deterioration of certain internal components (the CMOS battery, hard disk drive, and/or power supply unit). If this deterioration occurs, motorized movements of the system will become unavailable. Manual movements of the stand (longitudinal, transversal and rotational for ceiling mounted systems and rotational for floor mounted systems) and table longitudinal movements remain available. Imaging (X-ray) functionality remains available.
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 FD20/20 OR Table is used in surgical settings to assist in imaging and patient positioning during operations. It integrates motorized movements to position the operating table and imaging equipment.
Deterioration of key internal components can stop motorized movements, potentially affecting patient positioning during procedures; manual movements may still be possible, but the risk of incorrect positioning exists.
This recall is not described as part of a broader industry pattern in the provided data.
Hospitals may need to switch to manual positioning; potential workflow disruptions and increased clinician workload.
Refer to the FDA enforcement page linked in the recall notice for official instructions.
Refunds or replacements likely processed through Philips over weeks to months.
Keep all recall notices, incident reports, correspondence with the manufacturer, and replacement timelines.
Product: Allura Xper FD20/20 OR Table. Product Code: 722039. Associated 510(k) numbers: K102005, K130842, K130638, K133292, K141979, K161563, K162859, K033737, K041949. Quantity: 3 units (OUS only). Distribution: Worldwide. Countries listed include United States and many others across Europe, Asia, Africa, and the Americas.
No specific injuries or incidents are detailed in the provided recall notice.
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