Philips Allura Xper FD20/20 OR Table Recall: X-ray Imaging 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 Allura Xper FD20/20 OR Table systems with System Code 722039 because X-ray imaging may not start or may stop unexpectedly when using the wired foot switch. This could lead to incomplete medical imaging during procedures.

Why it’s dangerous

The wired foot switch may fail to initiate X-ray imaging properly, causing imaging to stop unexpectedly during procedures. This could result in incomplete medical imaging and potential delays in diagnosis or treatment.

Who’s affected

Medical facilities using the recalled Allura Xper FD20/20 OR Table systems with System Code 722039 are most at risk. Patients undergoing imaging procedures with these systems may be affected.

How to tell if you have this one

Check for System Code 722039 on the device. The system also has a unique device identifier (UDI) starting with 00884838054271 and a system serial number starting with 42586.

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 722039 to confirm if your device is affected.

✎ GovInfoNow

Questions people ask

Is this recall affecting my medical imaging equipment?

Yes, if your Allura Xper FD20/20 OR Table system has System Code 722039, it is affected.

How can I tell if my device is recalled?

Look for System Code 722039, UDI starting with 00884838054271, or system serial number starting with 42586.

What should I do if I have this device?

Check the system code to confirm if your device is affected. Philips does not provide a specific remedy for this recall.

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-1670-2026 — Philips Philips

Hello,

I own a Philips that is covered by recall Z-1670-2026 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-1670-2026 (March 3, 2026) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1670-2026 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 FD20/20 OR Table; System Code: 722039;

Use caution until it’s fixed