Medium risk Drugs & MedicationsClass II

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Recall

Allura Xper FD. Model Numbers: 722026, 722027, 722028, 722029, 722035, 722038, 722039, 722058. Interventional fluoroscopic x-ray system.

Updated June 29, 2026

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. is recalling Allura Xper FD. Model Numbers: 722026, 722027, 722028, 722029, 722035, 722038, 722039, 722058. Interventional fluoroscopic x-ray system.. Hazard: Firmware issue potentially leading to loss of geometry movements.

Is the PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. recalled? Yes. This product was recalled by FDA on June 29, 2026. Details below.

What is recalled

Allura Xper FD. Model Numbers: 722026, 722027, 722028, 722029, 722035, 722038, 722039, 722058. Interventional fluoroscopic x-ray system.

Am I affected

You may be affected if you own this product. Check the brand, model, and lot/date codes listed in the recall against your item.

What to do right now

Voluntary: Firm initiated

The hazard

Firmware issue potentially leading to loss of geometry movements.

Brands affected

Source
FDA
Category
Drugs & Medications
Recall ID
fda-Z-2928-2026
Classification
Class II
Recalled
June 29, 2026
Read the official notice

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