Philips Allura Xper FD20/20 X-ray System May Not Start Properly

Take action

Contact the company & request your remedy

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

No email on file — write to the address above instead.

✎ GovInfoNow plain-language explainer

What happened, in plain English

Philips is recalling all Allura Xper FD20/20 X-ray systems with System Code 722038 because the X-ray imaging may not start or may stop unexpectedly when using the wired foot switch. This could lead to incomplete medical imaging, which might affect diagnosis and treatment.

Why it’s dangerous

The X-ray imaging may not start or may stop intermittently when using the wired foot switch. This could result in incomplete medical imaging, potentially affecting diagnosis and treatment outcomes.

Who’s affected

Medical facilities using the Allura Xper FD20/20 X-ray system with System Code 722038 are most at risk. Patients undergoing X-ray procedures may experience incomplete imaging if the system fails to initiate properly.

How to tell if you have this one

Check for System Code 722038 on the device. The system also has a unique identifier (UDI) starting with 00884838054226 and a specific serial number pattern.

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 722038 to confirm if the device is affected.

✎ GovInfoNow

Questions people ask

Why is this system being recalled?

Philips identified instances where X-ray imaging may not initiate or may occur intermittently when using the wired foot switch.

How can I tell if my system is affected?

Check for System Code 722038 on the device. The system also has a unique identifier (UDI) starting with 00884838054226 and a specific serial number pattern.

What should I do if I have this system?

The recall does not specify a remedy, so contact Philips directly for guidance.

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-1669-2026 — Philips Philips

Hello,

I own a Philips that is covered by recall Z-1669-2026 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.

Similar recalls

From people who’ve dealt with this

Experiences, tips, and questions from readers. Every comment is reviewed before it appears.

No comments yet — be the first to share your experience.

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-1669-2026 (March 3, 2026) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1669-2026 to see it in context.
Plain-language summary written by qwen3:4b on August 10, 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 FD20/20; System Code: 722038;

Lower-risk recall