The Recall Desk
ModerateFDA (Devices)·Z-2634-2025·Announced 2025-10-01

Philips OR Table motorized movements may fail due to component deterioration

Philips Allura Xper FD20/15 OR Tables may lose motorized movements due to deterioration of internal components including battery, hard drive, and power supply. Manual movements and imaging functionality remain available.

What this means for you

Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.

Our severity reasoning: FDA Class II classification applies. No illnesses, injuries, or deaths have been reported. The hazard is functional degradation with significant mitigating factors—manual operation and imaging remain fully available—consistent with a precautionary moderate-severity recall.

Plain-English summary

The Philips Allura Xper FD20/15 OR Table is a motorized operating room table used in surgical facilities. The recalled units may experience deterioration of internal components, specifically the CMOS battery, hard disk drive, and/or power supply unit. When this deterioration occurs, the motorized movements of the system become unavailable. For ceiling-mounted systems, motorized longitudinal, transversal, and rotational movements are affected. For floor-mounted systems, motorized rotational movement is affected.

Despite the loss of motorized functionality, manual movements of the stand remain available, as do manual table longitudinal movements and all X-ray imaging capabilities. This means surgical teams can continue to position the table using manual controls.

The recalled Allura Xper FD20/15 OR Table has been distributed worldwide, including throughout the United States. It is manufactured by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. and identified by product code 722059. Hospitals and surgical facilities using this equipment should contact Philips Medical Systems for information about identifying affected units and receiving repair or remedy.

The recalled product

Product
Allura Xper FD20/15 OR Table; Product Code: 722059; Associated 510(k) numbers: K102005, K130842, K130638, K133292, K141979, K161563, K162859, K033737, K041949;
Manufacturer
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Category
Medical Device — Operating Room Equipment
Hazard
  • component-deterioration
  • functional-degradation

Is your product affected?

Check your packaging against the codes below. If any of them match, the product is part of this recall.

Lot numbers (3)

  • Product Code: 722059
  • UDI-DI: 00884838059122
  • Serial numbers: 2

Distribution

Distributed nationwide across the United States.

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