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Medical Device

Philips Patient Information Center iX REF:866389

Recall date: 2026-09-23 · Source: FDA_DEVICE
Brand / Firm
Philips North America
Product
Philips Patient Information Center iX REF:866389
Reason for recall
Due to software malfunction, patient information system may freeze and become unresponsive.
Units affected
7359 Units
Description
Philips Patient Information Center iX REF:866389
View official recall notice →