Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Patient Information Center iX Recalled by Philips North America Due to A recent software (SW) patch modifies Mobile Event...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Philips North America directly.
Affected Products
Patient Information Center iX; Software Version Number: 4.5.0
Quantity: 146 units (41 US, 105 OUS)
Why Was This Recalled?
A recent software (SW) patch modifies Mobile Event Notification filter settings without providing any indication to the user when upgrading the system.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Philips North America
Philips North America has 107 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report