Philips Medical Systems Nederland B.V. recalls 4 units of the Allura Xper FD20 Biplane OR Table after identifying intermittent or failed X-ray initiation when using the wired foot switch. The recall covers System Codes 722020 and 722025. Healthcare facilities were notified by letter. Stop using the affected devices and follow Philips 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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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.
The wired foot switch may fail to initiate imaging or do so intermittently, potentially delaying or complicating procedures.
This recall is not described as part of a broader industry pattern.
Hospitals may experience imaging delays or interruptions. The recall affects only four units but involves global distribution, necessitating prompt action by facilities.
Check the device labeling for System Code and Serial Number. Refer to the FDA recall page linked in the notice.
Most recall-related refunds or replacements are processed within 4-8 weeks after the retailer or manufacturer confirms eligibility.
Keep the recall notice, device ID labels, serial numbers, correspondence with Philips, and any replacement or refund confirmations.
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.
No injuries or incidents have been reported.
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