HIGH

Philips Recalls Allura Xper FD20 OR Table Due to Electrical Hazard

Philips recalled four units of the Allura Xper FD20 OR Table on December 15, 2025, due to a potential electrical hazard. The drip tray installation issues could allow coolant to contact electrical components, risking short-circuits and system shutdowns. Healthcare providers and patients must stop using the device immediately.

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

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

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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

  1. Check the model number on your device; it should read 722023.
  2. Look for serial numbers 10, 85, or 125 to confirm if your unit is affected.
  3. 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.

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
  • Worldwide distribution
  • Potential for electrical short-circuits

Safety Guide

Not sure what to do next? Our guide walks you through the process step by step.

Read: What to Do When You Find a Recalled Product

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Safety Assessment

Risk LevelHIGH
Severity Score
8/ 10
Affected Groups
GENERAL
Injury Types
ELECTRICAL

Product Details

Model Numbers
Model Number: 722023
System Product Name: Allura Xper FD20 OR Table
UDI-DI: 00884838059085
Serial Numbers: 103
10
+2 more
Affected States
ALL
Report Date
January 21, 2026
Recall Status
ACTIVE

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