Use cautionMedical device recall · FDA · Published July 19, 2023
Philips Allura Xper Series Recall: Unintended Radiation Risk
Philips recalls Allura Xper series devices due to risk of unintended radiation emission when foot switch pedal gets stuck. Affected units may cause radiation exposure during use.
“Philips Allura Xper Series Recall: Unintended Radiation Risk.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/57627-philips-allura-xper-series-recall-unintended-radiation-risk. Based on FDA recall #Z-2402-2023 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2402-2023%22&limit=1).
The FDA announced on July 19, 2023, that Philips Medical Systems Nederland B.V. is recalling Allura Xper series systems due to a foot switch pedal hazard. The device may emit unintended radiation if the pedal gets stuck in the active position.
How to tell if you have it
Brand: Philips
Product: Allura Xper series
Quantity: 5432 systems
The hazard
A foot switch pedal may get stuck in the active position when the user releases the pedal, resulting in the emission of unintended radiation. The FDA classified this as a Class II recall.
Context
GovInfoNow's records show PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. has 58 other recalls on record since May 26, 2021. Other recent recalls of similar products include Philips Brilliance CT 64 Medical Scanner Recall (August 7, 2026), Philips IQon Spectral CT Software 4.7.7.x Recall (August 7, 2026), and Philips Ingenuity CT Scanners (August 7, 2026).
How to tell if you have this one
Check if your Philips device has the Allura Xper series name. The recall applies to all units sold by Philips Medical Systems Nederland B.V.
Brand
Philips
Category
Medical device
FDA recall event · 3 products
All 3 products in this recall
FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.
Classification
Class II
Status
Ongoing
Distribution
US Nationwide Distribution
Recall number
Product, codes & lots
Z-2402-2023
Allura Xper series; Allura Xper series
Z-2403-2023
Azurion; Azurion series
Z-2404-2023
MultiDiagnost-Eleva; MultiDiagnost-Eleva
Based on the official FDA remedy
What to do — step by step
Check Device Status
Verify if your device is part of the Allura Xper series by checking the product label or documentation.
Where it went and when
Where it was distributed
Distributed nationwide.
Nationwide
Not listed
FDA distribution: “US Nationwide Distribution” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide.
Recall timeline
FDA published this recall 56 days after the firm started it.
1Firm started the recall
2FDA classified it Class II
3Published in FDA’s Enforcement Report
Dates from the agency record only; steps without a date are left out.
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-2402-2023 (July 19, 2023) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-2402-2023 to see it in context.
Plain-language summary written by qwen3:4b on August 19, 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.