Philips recalls X-ray imaging systems with specific serial numbers due to potential failure to initiate X-ray imaging when using the wired foot switch.
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 all ALLURA Xper FD10/10 X-ray systems with specific serial numbers because they may not start X-ray imaging properly when using the wired foot switch. This could lead to incomplete scans or missed diagnoses.
The X-ray system may fail to initiate or intermittently occur X-ray imaging when the wired foot switch is used. This could result in incomplete scans or missed diagnoses during medical procedures.
Healthcare professionals using the ALLURA Xper FD10/10 X-ray systems with the listed serial numbers are most at risk. Patients using these systems may experience incomplete imaging.
Check the system code (722005, 722011, or 722027) and the serial numbers listed in the recall notice. The system code and serial numbers are provided in the product description.
Identify the system code (722005, 722011, or 722027) and corresponding serial numbers listed in the recall notice.
The ALLURA Xper FD10/10 X-ray system with system codes 722005, 722011, and 722027.
Philips has identified instances where the X-ray imaging may not be initiated or may occur intermittently when using the wired foot switch.
Check the system code (722005, 722011, or 722027) and the serial numbers listed in the recall notice.
We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.
Subject: Recall Z-1662-2026 — Philips Philips Hello, I own a Philips that is covered by recall Z-1662-2026 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
