Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Philips IntelliVue Module Measurement X2 Model: M3002A Recalled by Philips Electronics North America Corporation Due to The ST elevation alarm on the Patient Monitor...
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 Electronics North America Corporation directly.
Affected Products
Philips IntelliVue Module Measurement X2 Model: M3002A
Quantity: 13,300
Why Was This Recalled?
The ST elevation alarm on the Patient Monitor or standalone X2 Measurement Module will not sound when indicated for all chest leads derived using Hexad 12-Lead ECG Monitoring in the Host Monitor
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Philips Electronics North America Corporation
Philips Electronics North America Corporation has 160 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report