Philips ALLURA Xper FD10F X-ray System May Not Start Properly

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Recalling firmPHILIPS MEDICAL SYSTEMS NEDERLAND B.V.Veenpluis 6 · Best, N/A

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✎ GovInfoNow plain-language explainer

What happened, in plain English

Philips is recalling all ALLURA Xper FD10F X-ray systems with system code 722002 because they may not start X-ray imaging properly when using the wired foot switch. This could lead to incomplete scans or repeated attempts, affecting medical procedures.

Why it’s dangerous

The X-ray system may fail to initiate or intermittently stop X-ray imaging when the wired foot switch is used. This could cause repeated attempts or incomplete scans during medical procedures, potentially delaying treatment.

Who’s affected

Medical facilities using the ALLURA Xper FD10F X-ray system with system code 722002 are most at risk. Patients undergoing X-ray procedures with this system could experience incomplete scans.

How to tell if you have this one

Check for the system code 722002 on the device. The system serial number starts with 53, 61, 78, 38, 28, 63, 3, 81, 66, 40.

Brand
Philips
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check System Code
Verify the system code is 722002 to confirm if the device is affected.

✎ GovInfoNow

Questions people ask

Is this recall affecting patients?

Yes, patients undergoing X-ray procedures with this system could experience incomplete scans.

How can I check if my system is affected?

Check for the system code 722002 on the device. The system serial number starts with 53, 61, 78, 38, 28, 63, 3, 81, 66, 40.

What should I do if I have this system?

The recall does not specify a remedy, so contact Philips for further instructions.

Take action

Contact Philips

We’ve drafted a message you can send Philips to request your refund or repair — edit it as you like.

✉️ Open in email

Subject: Recall Z-1660-2026 — Philips Philips

Hello,

I own a Philips that is covered by recall Z-1660-2026 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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Where this comes from

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.

Official source: FDA Recall #Z-1660-2026 (March 3, 2026) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1660-2026 to see it in context.
Plain-language summary written by qwen3:4b on August 18, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalls ALLURA Xper FD10F; System Code: 722002;

Lower-risk recall