Philips Medical Systems Nederland B.V. recalled 196 ALLURA Xper FD20 OR Tables sold to hospitals nationwide and internationally. The defect may prevent X-ray imaging from starting or cause intermittent operation when using the wired foot switch. Hospitals should stop using the devices and follow the recall instructions sent by letter.
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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The ALLURA Xper FD20 OR Table is an operating room X-ray table used in interventional radiology and surgical procedures.
A fault in the wired foot switch can prevent imaging from starting or cause intermittent operation, potentially delaying diagnosis and treatment.
This recall is not described as part of a broader industry pattern in the notice.
Hospitals may need to halt procedures requiring immediate imaging and implement alternative imaging workflows while awaiting remediation.
Recall notifications and device labels typically show System Code and Serial Number.
Remediation timelines vary; hospitals should follow manufacturer guidance and FDA recall updates.
Keep copies of recall notices, correspondence with Philips, and any replacement/repair records.
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
No injuries or incidents have been reported.
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