Is my device affected by this recall?

The recall covers Allura Xper FD20 Biplane OR Tables with System Code 722020 or 722025. Four units are affected globally. Check your device's System Code and System Serial Number.

X-ray imaging may not initiate or may start intermittently when using the wired foot switch.

How do I identify if my device is affected?

Look for System Code 722020 or 722025 and System Serial Numbers 4 or 6 on the device labeling.

Will there be a refund or replacement?

Philips will provide recall instructions. The recall notice mentions a remedy; follow the official guidance for refunds or replacements.

Where can I get more information?

See the FDA enforcement report page for this recall; recall notification letters are distributed to facilities.

Are there injuries reported?

No injuries or incidents have been reported to date.

What if the manufacturer is slow to respond?

Escalate via hospital risk management and regulator reporting channels and document all communications.

Is this recall part of a broader pattern?

The notice does not indicate a broader industry pattern beyond this device family.

What should hospitals document during this recall?

Document device IDs, serial numbers, batch information, communications with Philips, and recall newspaper or letter notifications.

HIGHMarch 3, 2026

Philips Allura Xper FD20 Biplane OR Table Recall for 4 Units Over Intermittent X-ray Activation (202

Q: What should I do now?

Stop using the device immediately and contact Philips Medical Systems Nederland B.V. or your healthcare provider for instructions. Follow the recall letter.

Philips Medical Systems Nederland B.V. recalls 4 units of the Allura Xper FD20 Biplane OR Table after identifying intermittent or failed X-ray initiation when using the wired foot switch. The recall covers System Codes 722020 and 722025. Healthcare facilities were notified by letter. Stop using the affected devices and follow Philips instructions.

Quick Facts at a Glance

Recall Date: March 3, 2026
Hazard Level: HIGH
Brand: Philips Medical Systems Nederland
Category: Health & Personal Care
Sold At: Unknown
Geographic Scope: 1 states
At-Risk Groups: GENERAL

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 Biplane OR Table is used in interventional radiology settings to perform X-ray guided procedures. Hospitals rely on precise imaging during catheter-based interventions.

Why This Is Dangerous

The wired foot switch may fail to initiate imaging or do so intermittently, potentially delaying or complicating procedures.

Industry Context

This recall is not described as part of a broader industry pattern.

Real-World Impact

Hospitals may experience imaging delays or interruptions. The recall affects only four units but involves global distribution, necessitating prompt action by facilities.

Practical Guidance

How to identify if yours is affected

1) Locate System Code on your device (722020 or 722025).
2) Check System Serial Number (4 for 722020; 6 for 722025).
3) Confirm whether a UDI exists and compare with 00884838059108 (for 722025).
4) Review recall notification letter for instructions.

Where to find product info

Check the device labeling for System Code and Serial Number. Refer to the FDA recall page linked in the notice.

What timeline to expect

Most recall-related refunds or replacements are processed within 4-8 weeks after the retailer or manufacturer confirms eligibility.

If the manufacturer is unresponsive

Contact hospital risk management.
File a consumer safety complaint with regulatory agencies if needed.
Document every outreach and response from Philips.

How to prevent similar issues

Ensure service agreements include monitoring for recall notices.
Establish internal recall response procedures for imaging equipment.
Before procurement, verify recall history and post-market surveillance reports.

Documentation advice

Keep the recall notice, device ID labels, serial numbers, correspondence with Philips, and any replacement or refund confirmations.

Product Details

Model codes: (1) System Code 722020; (2) System Code 722025. System Serial Numbers: 4 and 6 respectively. UDI: 00884838059108 for the 722025 system. Sold through nationwide domestic distribution and international channels in more than 60 countries, with a broad hospital and imaging-center user base. Quantity recalled: 4 units (2 in the US, 2 outside the US). Sold to healthcare providers by Philips Medical Systems Nederland B.V. Unknown price information. Recall date: 2026-03-03. Report date: 2026-04-08. Status: ACTIVE.

Reported Incidents

No injuries or incidents have been reported.

Key Facts

4 units recalled (2 US, 2 international)
System Codes 722020 and 722025
System Serial Numbers 4 and 6
UDI for 722025: 00884838059108
Global distribution across 60+ countries
Recall date 2026-03-03; Report date 2026-04-08

View Original Recall on FDA - Medical Devices

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Safety Guide

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Safety Assessment

Risk LevelHIGH

Severity Score

8/ 10

Affected Groups

GENERAL

Injury Types

ELECTRICALOTHER

Product Classification

CategoryHealth & Personal Care › Medical Imaging Equipment

Product TypeX-ray imaging table

Product Details

Sep 3, 2025

Philips Medical Systems Nederland

The BIOS