HIGH

Philips Allura Xper FD20/15 OR Table Recall for 8 Units Worldwide in 2026

Philips Medical Systems Nederland B.V. recalls 8 Allura Xper FD20/15 OR Tables worldwide due to a risk that X-ray imaging may not start or may stop intermittently when using the wired foot switch. The issue is tied to System Code 722059 and requires immediate action. Hospitals and patients should stop using the device and follow the manufacturer’s recall instructions.

Quick Facts at a Glance

Recall Date
March 3, 2026
Hazard Level
HIGH
Brand
Philips
Category
Health & Personal Care
Sold At
Multiple Retailers
Geographic Scope
1 states
At-Risk Groups
GENERAL, PREGNANT, PREGNANT

Hazard Information

Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.

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 FD20/15 OR Table is part of Philips’ interventional radiology system used in operating rooms for imaging-guided procedures.

Why This Is Dangerous

A wired foot switch is used to initiate X-ray imaging. Malfunction can prevent imaging from starting or cause intermittent imaging, potentially impacting procedures.

Industry Context

This recall is not described as part of a broader industry pattern in the provided data.

Real-World Impact

Hospitals and clinics may need to halt use of affected tables and coordinate with Philips for remediation, potentially affecting scheduling and patient throughput.

Practical Guidance

How to identify if yours is affected

  1. 1. Locate the System Code on the device label
  2. 2. Verify UDI 00884838059122
  3. 3. Check System Serial Number against the recall list
  4. 4. Reference the recall notification letter for instructions

Where to find product info

Recall letters and Philips official recall pages; UDI and System Code appear on device labels and documentation

What timeline to expect

4-8 weeks for recall remediation processes

If the manufacturer is unresponsive

  • Escalate to hospital risk management
  • Document all communications
  • Consult regulatory requirements if the vendor is slow to respond

How to prevent similar issues

  • Maintain updated device inventories with System Codes and UDIs
  • Coordinate with biomedical teams for rapid recall actions
  • Ensure clear recall communication protocols in hospitals

Documentation advice

Keep the recall letter, capture photos of device labels, log all communications with Philips and hospital staff

Product Details

Product: Allura Xper FD20/15 OR Table System Code: 722059 UDI: 00884838059122 System Serial Number: 33; other listed identifiers include 7, 35, 40, 38, 41, 37, 2 Quantity: 8 units recalled (2 US, 6 outside the US) Distribution: Domestic nationwide and international across many countries including Afghanistan, Albania, Algeria, Argentina, Armenia, Australia, Austria, and others Recall Date: 2026-03-03 Report Date: 2026-04-08 Manufacturer: Philips Medical Systems Nederland B.V.

Reported Incidents

No injuries or incidents have been reported.

Key Facts

  • 8 units recalled worldwide (2 US, 6 international)
  • System Code 722059
  • UDI 00884838059122
  • No injuries or incidents reported
  • Recall date 2026-03-03; status ACTIVE

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
6/ 10
Affected Groups
GENERALPREGNANTPREGNANTGENERAL
Injury Types
OTHER

Product Details

Brand
Model Numbers
System Code: 722059
UDI: 00884838059122
System Serial Number: 33
7
35
+5 more
Affected States
ALL
Report Date
April 8, 2026
Recall Status
ACTIVE

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