Philips Medical Systems Netherlands B.V. recalled three Allura Xper FD20/20 OR Tables on September 3, 2025. The recall addresses potential failures in internal components that could impede motorized functions. Users must stop using the device immediately and follow recall instructions.
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
The recalled product is the Allura Xper FD20/20 OR Table, Product Code 722039. It has associated 510(k) numbers K102005, K130842, K130638, K133292, K141979, K161563, K162859, K033737, and K041949. The product was distributed worldwide.
The operating room table may fail due to deterioration of internal components like the CMOS battery, hard disk drive, or power supply unit. If this occurs, motorized movements become unavailable, potentially impacting patient safety.
There are no reported injuries or incidents related to this recall. The manufacturer advises immediate cessation of use to prevent any potential risks.
Stop using the operating room table immediately. Follow the recall instructions provided by Philips Medical Systems. Contact your healthcare provider or Philips for further instructions.
For more information, contact Philips Medical Systems Netherlands B.V. through their official website or customer service.
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