Philips Allura Xper FD20 Operating Room Table Motorized Movement Failure
Philips Allura Xper FD20 operating room tables may lose motorized movement capability due to internal component deterioration. Manual positioning and imaging remain available.
What this means for you
Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.
Our severity reasoning: FDA Class II medical device recall where internal component deterioration may cause loss of motorized movements in operating room tables used during critical patient procedures. No injuries or illnesses have been reported, making this a risk-of-harm product where injury has not yet been reported.
Plain-English summary
Philips Medical Systems Nederland B.V. is recalling Allura Xper FD20 Biplane Operating Room Tables (product codes 722020 and 722025) due to potential deterioration of internal components including the CMOS battery, hard disk drive, and/or power supply unit.
If component deterioration occurs, motorized movements of the table will become unavailable. Manual positioning and X-ray imaging functionality remain available. The specific motorized movements affected depend on the installation type: ceiling-mounted systems lose longitudinal, transversal, and rotational movements, while floor-mounted systems lose rotational movement.
The recall affects 5 units total: 2 in the United States and 3 distributed outside the United States to numerous countries worldwide.
The recalled product
- Product
- Allura Xper FD20 Biplane OR Table Product Codes: (1)722020, (2) 722025; Associated 510(k) numbers: K102005, K130842, K130638, K133292, K141979, K161563, K162859, K033737, K041949;
- Manufacturer
- PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
- Hazard
- component-failure
- motorized-movement-loss
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 (9)
- Product Codes: (1)722020
- (2) 722025
- UDI-DI: (1) N/A
- (2) 00884838059108
- Serial numbers: (1) 6
- 4
- (2) 2
- 3
- 6
Distribution
Distributed nationwide across the United States.
Related recalls
Same category
- HighGE CARESCAPE Telemetry Server may lose patient ECG and oxygen saturation monitoring
FDA (Devices) · 2026-06-03
- HighGE APEXPRO and CARESCAPE Telemetry Systems Risk Loss of Patient Monitoring
FDA (Devices) · 2026-06-03
- SevereMedline Spinal Trays Recalled Due to Quality and Efficacy Concerns
FDA (Devices) · 2026-06-03
- HighPhilips Azurion and Allura Imaging Systems Recalled for Hard Drive Degradation
FDA (Devices) · 2026-06-03
- HighPhilips Allura Imaging Systems Hard Drive Degradation Affects Functionality
FDA (Devices) · 2026-06-03