Quick Facts at a Glance
- Recall Date
- September 3, 2025
- Hazard Level
- HIGH
- Brand
- Philips Medical Systems Netherlands B.V.
- Category
- Health & Personal Care
- Sold At
- Multiple Retailers
- Geographic Scope
- 1 states
- At-Risk Groups
- GENERAL, PREGNANT, PETS
What to Do Now
Use this page like a recall checklist: verify the product first, then act on the official remedy.
Immediate steps
- 1Stop using the product until you confirm whether it is included in the recall.
- 2Compare the product label, model number, UPC, color, size, and purchase location against the identifiers below.
- 3Follow the official remedy from FDA - Medical Devices; save photos, receipts, labels, and correspondence before contacting the company.
- 4If the product could harm a child, older adult, pet, or patient, move it out of reach immediately.
Check these identifiers
- Brand
- Philips Medical Systems Netherlands B.V.
- Product type
- Imaging/Diagnostic Equipment (OR Table)
- Model numbers
- Product Code: 722039, UDI-DI: 00884838054271, Serial numbers: 2, 4, 5
- Sold at
- Multiple Retailers
- Where affected
- ALL
Recall Timeline
Key dates and source checks for this recall record.
Recall announced
September 3, 2025
Reported by FDA DEVICE
October 1, 2025
RecallRadar source check
April 18, 2026
Consumer action
Use the official remedy and keep documentation.
Hazard Information
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.
What You Should Do
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
About This Product
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.
Why This Is Dangerous
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.
Industry Context
This recall is not described as part of a broader industry pattern in the provided data.
Real-World Impact
Hospitals may need to switch to manual positioning; potential workflow disruptions and increased clinician workload.
Practical Guidance
How to identify if yours is affected
- Check Product Code 722039 and UDI-DI 00884838054271 on the device label.
- Review serial numbers for 2, 4, or 5.
- Confirm recall status via manufacturer communications.
Where to find product info
Refer to the FDA enforcement page linked in the recall notice for official instructions.
What timeline to expect
Refunds or replacements likely processed through Philips over weeks to months.
If the manufacturer is unresponsive
- Escalate contact attempts within the hospital procurement or risk management teams.
- File formal complaints with the manufacturer and the FDA if needed.
How to prevent similar issues
- Verify follow-up service availability before purchasing imaging tables.
- Maintain device software and component life-cycle tracking.
- Establish contingency plans for equipment downtime.
Documentation advice
Keep all recall notices, incident reports, correspondence with the manufacturer, and replacement timelines.
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Product Details
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.
Reported Incidents
No specific injuries or incidents are detailed in the provided recall notice.
Key Facts
- 3 units recalled (OUS only)
- CMOS battery, HDD, and/or PSU deterioration
- Motorized movements may fail
- Imaging (X-ray) remains available
- Active recall as of 2025-10-01
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Safety Guide
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