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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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.
Philips says the wired foot switch may fail to initiate X-ray imaging or may do so intermittently. The issue could impair imaging during procedures.
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) Refer to the recall letter for detailed steps and any required device removal. 4) Follow the recall process until a resolution is provided.
Recall URL: https://www.accessdata.fda.gov/scripts/enforcement/enforce_rpt-Product-Tabs.cfm?recall_number=Z-1666-2026. Notification by letter. Manufacturer: Philips Medical Systems Nederland B.V.
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