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
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
- Product type
- Interventional Radiology Table
- Model numbers
- System Code: 722059, UDI: 00884838059122, System Serial Number: 33, 7, 35, 40, 38, 41 +2 more
- Sold at
- Multiple Retailers
- 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 FD20/15 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. Locate the System Code on the device label
- 3. Check System Serial Number against the recall list
- 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
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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)
- No injuries or incidents reported
- Recall date 2026-03-03; status ACTIVE
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Safety Guide
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