Philips Allura Xper FD20/20 Operating Room Table Motorized Movement Failure
Philips Allura Xper FD20/20 OR tables may lose motorized movement capability due to internal component deterioration. Manual positioning and imaging functions remain available. FDA Class II recall affects 3 units outside the United States.
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 device with component deterioration causing loss of motorized functionality. No illnesses, injuries, or deaths reported in the source. Manual positioning and imaging remain available, reducing patient harm risk.
Plain-English summary
The Philips Allura Xper FD20/20 OR Table is a surgical operating room table with integrated X-ray imaging capability. It is subject to an FDA Class II recall issued by manufacturer Philips Medical Systems Nederland B.V.
The recall is due to deterioration of internal components, including the CMOS battery, hard disk drive, and/or power supply unit. When deterioration occurs, motorized movements of the table system become unavailable. This includes longitudinal (front-to-back), transversal (side-to-side), and rotational positioning on ceiling-mounted systems, or rotational positioning on floor-mounted systems. However, manual operation of these movements remains functional, and the X-ray imaging capability is unaffected.
The recall affects 3 units distributed outside the United States. Healthcare facilities using affected equipment should contact Philips Medical Systems Nederland B.V. for guidance on service options and component replacement. While motorized positioning may not be available, the table remains operationally functional through manual positioning and continues to support imaging-guided procedures.
The recalled product
- Product
- Allura Xper FD20/20 OR Table; Product Code: 722039; Associated 510(k) numbers: K102005, K130842, K130638, K133292, K141979, K161563, K162859, K033737, K041949;
- Manufacturer
- PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
- Hazard
- motorized-movement-failure
- component-deterioration
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 (5)
- Product Code: 722039
- UDI-DI: 00884838054271
- Serial numbers: 2
- 4
- 5
Distribution
Distributed nationwide across the United States.
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