Reported Jun 24, 2026 · Ongoing

Philips Allura Xper with the following Model Numbers: Model # 722001 for Allura Xper FD10C; Model # 722002 for Allura…

Philips Medical Systems Nederland B.v.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. · Veenpluis 4-6 · Best · N/A

Is this the product you have?

26 of 26 products

Products covered by this recall
Model / numberProduct as published
722001Philips Allura Xper with the following Model Numbers: for Allura Xper FD10C
722002for Allura Xper FD10F
722003for Allura Xper FD10
722005for Allura Xper FD10/10
722006for Allura Xper FD20
722008for Allura Xper FD20 Biplane
722010for Allura Xper FD10
722011for Allura Xper FD10/10
722012for Allura Xper FD20
722013for Allura Xper FD20 Biplane
722015for Allura Xper FD20 OR Table
722019for Allura Xper FD10/10 OR Table
722020for Allura Xper FD20 Biplane OR Table
722022for Allura Xper FD10 OR Table
722023for Allura Xper FD20 OR Table
722025for Allura Xper FD20 Biplane OR Table
722026for Allura Xper FD10
722027for Allura Xper FD10/10
722028for Allura Xper FD20
722029for Allura Xper FD20/10
Lot codes and dates
  • All codes

This recall covers 2 products

The agency filed one notice per product. You are reading one of them; the other one is below.

Why it was recalled

Philips Allura Xper and MultiDiagnost-Eleva systems Hand switch button not fully releasing potentially leading to loss of imaging functionality or unintended radiation exposure and additional contrast injection

This product could cause temporary or reversible health problems — stop using it.

Want the full recall guide?

The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.

Free recall alerts

Get alerted about new Philips Medical Systems Nederland B.v. recalls

One email when a matching recall is published. No account, no cost, unsubscribe in one click.

Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Data as of Sep 19, 5:41 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.