Quick Facts at a Glance
- Recall Date
- December 15, 2025
- Hazard Level
- HIGH
- Brand
- PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
- Category
- Health & Personal Care
- Sold At
- Multiple Retailers
- Geographic Scope
- 1 states
- At-Risk Groups
- GENERAL
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 NEDERLAND B.V.
- Product type
- OR Table
- Model numbers
- Model Number: 722023, System Product Name: Allura Xper FD20 OR Table, UDI-DI: 00884838059085, Serial Numbers: 103, 10, 85, 125
- Sold at
- Multiple Retailers
- Where affected
- ALL
Recall Timeline
Key dates and source checks for this recall record.
Recall announced
December 15, 2025
Reported by FDA DEVICE
January 21, 2026
RecallRadar source check
January 28, 2026
Consumer action
Use the official remedy and keep documentation.
Hazard Information
Philips has identified that in a limited number of impacted systems the drip tray beneath the cooling unit was not installed under previous field corrections, or evidence of the implementation was not adequately documented. If it is not installed, there is a potential for coolant liquid to contact electrical components. This could lead to electrical short-circuits, which may trigger system fuses and result in system shutdown.
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 OR Table is used in operating rooms for various medical procedures. It is designed to provide a stable and sterile environment for surgical operations, which is critical in healthcare settings.
Why This Is Dangerous
The hazard arises from the potential failure to install the drip tray, leading to coolant leaks. This can result in contact with electrical components, causing shorts that can disrupt the device's function.
Industry Context
This recall is not part of a broader industry pattern.
Real-World Impact
The recall affects only a few units, but the risk of electrical failure poses significant safety concerns for users in medical environments.
Practical Guidance
How to identify if yours is affected
- Check the model number on your device; it should read 722023.
- Look for serial numbers 10, 85, or 125 to confirm if your unit is affected.
- Refer to the recall notification letter for additional details.
Where to find product info
The model number and serial numbers are usually located on a label affixed to the device or in the user manual.
What timeline to expect
Expect a refund processing timeline of approximately 4-6 weeks after returning the device.
If the manufacturer is unresponsive
- Contact Philips again with your request.
- Document all communication and attempts to reach customer service.
How to prevent similar issues
- Ensure that medical devices are certified and compliant with safety standards before purchase.
- Regularly check for recalls on medical devices from manufacturers.
Documentation advice
Keep a record of all correspondence related to the recall, including emails and letters, as well as copies of any receipts.
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Product Details
The recall affects the Allura Xper FD20 OR Table, Model Number 722023. The recalled units have serial numbers 10, 85, and 125. The product was distributed worldwide, including the US and various countries.
Key Facts
- Recall date: December 15, 2025
- Reported date: January 21, 2026
- Quantity recalled: 4 units
- Potential for electrical short-circuits
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Safety Guide
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