Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Automated External Defibrillator - HeartStart MRx Monitor/Defibrillator Recalled by Philips Electronics North America Corporation Due to Philips MRx devices have an EtCO2 module that...
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
Automated External Defibrillator - HeartStart MRx Monitor/Defibrillator
Quantity: 20 units ( 18 domestic, 2 foreign)
Why Was This Recalled?
Philips MRx devices have an EtCO2 module that may contain contamination; this contamination (will/may) cause the device to be unable to display the EtCO2 or CO2 waveform (capnogram).
Where Was This Sold?
20 units affected. 18 domestic, 2 foreign.
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