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
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
- Product type
- X-ray imaging table
- Model numbers
- 722020, 722025
- Sold at
- Unknown
- Where affected
- ALL
Recall Timeline
Key dates and source checks for this recall record.
Recall announced
March 3, 2026
Reported by FDA DEVICE
April 8, 2026
RecallRadar source check
April 15, 2026
Consumer action
Use the official remedy and keep documentation.
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
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.
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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
- Global distribution across 60+ countries
- Recall date 2026-03-03; Report date 2026-04-08
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Safety Guide
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