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FDA
Food and Drug Administration · Recall Z-2258-2026 · Apr 30, 2026

Azurion system; System Code Description (Model Numbers): Azurion 3 M12 (722063, 722221), Azurion 3 M15 (722064, 722222), Azurion 5 M12 (722227), Azurion 5 M20 (722228), Azurion 7 B12 (722067, 722225), Azurion 7 B20 (722068, 722226), Azurion 7 M12 (722078, 722223), Azurion 7 M20 (722079, 722224).

PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

The hazard

It was identified that HDDs used in the PCs of Azurion and Allura systems may show a decrease in performance as they age, particularly beyond six years of service. Issues with an HDD may, depending on the specific system PC in which the affected HDD is installed, result in loss of imaging functionality. Additionally, in Allura systems, this may lead to loss of motorized movement, or loss of data. In some cases, a system restart may temporarily restore functionality. FDA Class II recall.

The remedy

Follow FDA guidance

About this recall

Azurion system; System Code Description (Model Numbers): Azurion 3 M12 (722063, 722221), Azurion 3 M15 (722064, 722222), Azurion 5 M12 (722227), Azurion 5 M20 (722228), Azurion 7 B12 (722067, 722225), Azurion 7 B20 (722068, 722226), Azurion 7 M12 (722078, 722223), Azurion 7 M20 (722079, 722224).

Affected identifiers

Check these against the label on your unit. An identifier match is how a recall is confirmed, not just suspected.

Model 1. Azurion 3 M12Model Model: 722063Model UDI: (01)00884838085275(21)122Model (01)00884838085275(21)64Model (01)00884838085275(21)56Model (01)00884838085275(21)131Model (01)00884838085275(21)84Model (01)00884838085275(21)132Model (01)00884838085275(21)98Model (01)00884838085275(21)108Model (01)00884838085275(21)77Model (01)00884838085275(21)82Model (01)00884838085275(21)47Model (01)00884838085275(21)80Model (01)00884838085275(21)146Model (01)00884838085275(21)102Model (01)00884838085275(21)117Model (01)00884838085275(21)2Model (01)00884838085275(21)149Model (01)00884838085275(21)99Model (01)00884838085275(21)44Model (01)00884838085275(21)3Model (01)00884838085275(21)28Model (01)00884838085275(21)144Model (01)00884838085275(21)62UPC 00884838085275

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Sourced from the Food and Drug Administration’s public recall data. Always verify serial and date ranges against the official notice before acting.