HomeMedical Device recalls
Medium severity

Patient Information Center iX; Software Version Number: 4.5.0

SourceFDA Device Enforcement
CategoryMedical Device
SeverityMedium
Statusongoing
Recall dateDecember 22, 2025
ReportedJanuary 28, 2026
Recalling firmPhilips North America
Country / regionUnited States MA

Hazard

A recent software (SW) patch modifies Mobile Event Notification filter settings without providing any indication to the user when upgrading the system.

Affected products

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