Official recall notice

FDA DeviceClass IINotable

FDA Recall: Philips Patient Information Center iX REF:866389

Recall date
2026-09-23
FDA class
Class II

Why it was recalled

Hazard

Due to software malfunction, patient information system may freeze and become unresponsive.

Product description

Due to software malfunction, patient information system may freeze and become unresponsive.

Affected products

All PIC iX software versions 4.0-4.5/UDI: (01)00884838127067

Verify with the official notice →
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