Philips recalls ALLURA Xper FD10 OR Table systems with specific serial numbers due to risk of improper X-ray imaging initiation. Affected units may require repair or replacement to ensure safe medical imaging.
Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
Philips is recalling ALLURA Xper FD10 OR Table systems with specific serial numbers because the X-ray imaging may not start or may work intermittently when using the wired foot switch. This could lead to incorrect medical imaging results if the system fails to initiate properly.
The wired foot switch may fail to initiate or intermittently trigger X-ray imaging during use. This could result in improper medical imaging if the system does not start correctly or stops working unexpectedly during a procedure.
Medical facilities using the ALLURA Xper FD10 OR Table system with the specified serial numbers are most at risk. Patients undergoing X-ray procedures with these systems could experience inaccurate imaging results.
Check for system codes 722022 or 722033 on the device. The system serial numbers are 6 and 1 respectively. These units were sold with specific UDI numbers.
Identify the system code on the device, which should be either 722022 or 722033.
Reach out to Philips for guidance on whether your unit is affected and what steps to take next.
Philips has identified instances where X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
Check for system codes 722022 or 722033. The system serial numbers are 6 and 1 respectively.
Contact Philips for guidance on whether your unit is affected and what steps to take next.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-1667-2026 — Philips Philips Hello, I own a Philips that is covered by recall Z-1667-2026 from Philips. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
