Quick Facts at a Glance
- Recall Date
- March 3, 2026
- 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
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 B.V.
- Product type
- Operating Room X-ray Table
- Model numbers
- 722015, 722023, 722035, Allura Xper FD20 OR Table
- 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 OR Table is an operating room X-ray table used in interventional radiology and surgical procedures.
Why This Is Dangerous
A fault in the wired foot switch can prevent imaging from starting or cause intermittent operation, potentially delaying diagnosis and treatment.
Industry Context
This recall is not described as part of a broader industry pattern in the notice.
Real-World Impact
Hospitals may need to halt procedures requiring immediate imaging and implement alternative imaging workflows while awaiting remediation.
Practical Guidance
How to identify if yours is affected
- Check System Code: 722015, 722023, or 722035 on the device label.
- Review System Serial Numbers associated with each code (e.g., 12, 16, 2, 8, 23, 3, 13 for 722015; 49, 41, 142, 110, 12, 179, 124, 27, 98 for 722023).
- Confirm the device is an ALLURA Xper FD20 OR Table.
Where to find product info
Recall notifications and device labels typically show System Code and Serial Number.
What timeline to expect
Remediation timelines vary; hospitals should follow manufacturer guidance and FDA recall updates.
If the manufacturer is unresponsive
- Document all attempts to contact the manufacturer.
- Escalate to hospital risk management and regulatory authorities if needed.
How to prevent similar issues
- Verify device safety status before use in any procedures.
- Keep recall communications accessible to clinical engineers and OR staff.
- If purchasing replacement, verify safety updates and firmware compatibility.
Documentation advice
Keep copies of recall notices, correspondence with Philips, and any replacement/repair records.
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Product Details
Product: ALLURA Xper FD20 OR Table System Codes: 722015, 722023, 722035 Quantity: 196 units (73 US, 223 OUS) Recall Date: 2026-03-03 Manufacturer: Philips Medical Systems Nederland B.V. Sold at: Hospitals and healthcare facilities via multiple distributors UDI: N/A System Serial Numbers: 722015 – 12, 16, 2, 8, 23, 3, 13; 722023 – 49, 41, 142, 110, 12, 179, 124, 27, 98 Status: ACTIVE Category: Class II recall Country of origin: Netherlands
Reported Incidents
No injuries or incidents have been reported.
Key Facts
- 196 units recalled (73 US, 223 OUS)
- Hazard: X-ray imaging may not start or may be intermittent when using wired foot switch
- Status: ACTIVE; Recall class II
- No injuries or incidents reported
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Safety Guide
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