PHILIPS recalls ALLURA Xper FD10 X-ray systems with specific system codes (722003, 722010, 722026) 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 X-ray systems with system codes 722003, 722010, and 722026 because the X-ray imaging may not start or may stop intermittently when using the wired foot switch. This could lead to incomplete medical imaging procedures.
The X-ray imaging may not initiate or may occur intermittently when using the wired foot switch. This could result in incomplete medical imaging procedures, potentially affecting diagnosis and treatment.
Medical facilities that own or use the ALLURA Xper FD10 X-ray systems with system codes 722003, 722010, or 722026 are most at risk. These systems are used in hospitals and clinics for medical imaging.
Check if your ALLURA Xper FD10 system has one of the following system codes: 722003, 722010, or 722026. The system code can be found in the system's documentation or on the device itself.
Identify your system code by checking the documentation or device label. The affected models have system codes 722003, 722010, or 722026.
Reach out to Philips customer support for further assistance or to confirm if your system is affected.
The affected system codes are 722003, 722010, and 722026.
Check your system code in the documentation or on the device label. If it matches 722003, 72210, or 722026, your system is affected.
Contact Philips customer support for further assistance or to confirm if your system is affected.
We’ve drafted a message you can send PHILIPS to request your refund or repair — edit it as you like.
Subject: Recall Z-1661-2026 — PHILIPS PHILIPS Hello, I own a PHILIPS that is covered by recall Z-1661-2026 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.
