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Philips North America recalls Patient Information Center iX; Software Version Number: 4.5.0
Recalled January 28, 2026 · FDA recall Z-1156-2026 · Philips North America
Hazard
A recent software (SW) patch modifies Mobile Event Notification filter settings without providing any indication to the user when upgrading the system. · FDA Class II
Units
146 units (41 US, 105 OUS)
Sold at
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.
Description
A recent software (SW) patch modifies Mobile Event Notification filter settings without providing any indication to the user when upgrading the system.
Product
Patient Information Center iX; Software Version Number: 4.5.0
Manufacturer(s)
Philips North America
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →