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.
Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
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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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.
The wired foot switch can fail to initiate X-ray imaging or do so intermittently. The malfunction may occur during interventional procedures, potentially delaying imaging that clinicians rely on.
No injuries or incidents have been reported.
1. Stop using the product. 2. Contact Philips Medical Systems Nederland B.V. or your healthcare provider for instructions. 3. Follow the recall letter for the remedy. 4. Ask about refunds or replacement options as provided by Philips.
Phone: Unknown Website: https://www.philips.com Hours: Unknown
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