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January 22, 2026
22
Jan

FDA Recall: Software patch notification error

January 22, 2026
Company: Phillips North America Date of Enforcement Report: 01/22/2026 Class: II PRODUCT: Patient Information Center iX; Software Version Number: 4.5.0 Recall Number: Z-1156-2026 REASON: A recent software (SW) patch modifies Mobile Event Notification filter settings without providing any indication to the user when upgrading the system. RECALLING FIRM/MANUFACTURER: Philips North America VOLUME: 146 units (41...
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