Medical Device Recall: Patient Information Center iX; Software Version Number: 4.5.0
Philips North America · December 22, 2025
Reason for Recall
A recent software (SW) patch modifies Mobile Event Notification filter settings without providing any indication to the user when upgrading the system.
Distribution
Worldwide distribution - US Nationwide and the countries of Austria, Belgium, Brazil, Canada, Czech Republic, Dominican Rep, Finland, France, Germany, Greece, Hungary, India, Italy, Japan, Jordan, Netherlands, Norway, Poland, Saudi Arabia, Singapore, South Africa, South Korea, Spain, Sweden, Switzerland, Taiwan, United Kingdom, Utd.Arab.Emir.
States Affected
NATIONWIDE
Quantity Affected
146 units (41 US, 105 OUS)
Source: FDA (openFDA Device Enforcement)
Recall number: Z-1156-2026
Status: ongoing
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