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
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