Official recall notice

FDA DeviceClass IINotable

FDA Recall: Philips PIC iX Essentials REF:867093

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)00884838122772

Verify with the official notice →
Share:

Related Recalls

2026-09-23 · FDA_DEVICE
FDA Recall: Philips Patient Information Center iX REF:866389
Philips North America
2026-05-06 · FDA_DEVICE
FDA Recall: Philips Ingenia Ambition X with MR Elastography (MRE). 1. Model Number (REF): 781356. 2. Mod
Philips North America
2026-05-06 · FDA_DEVICE
FDA Recall: Philips SmartPath to dStream for 3.0T with MR Elastography (MRE). 1. Model Number (REF): 782145.
Philips North America
2026-05-06 · FDA_DEVICE
FDA Recall: Philips Upgrade to MR 7700 with MR Elastography (MRE). 1. Model Number (REF): 782130.
Philips North America