Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
IntelliVue Patient Monitor MX400. Model Number: 866060 Recalled by Philips North America Llc Due to Potential failure to alarm for "No Device Data"...
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 Llc directly.
Affected Products
IntelliVue Patient Monitor MX400. Model Number: 866060
Quantity: 28 units
Why Was This Recalled?
Potential failure to alarm for "No Device Data" INOP. The device to alarm after a Hamilton ventilator is disconnected from the EC10 Module or IntelliBridge I/O board.
Where Was This Sold?
US distribution to Florida, North Carolina, and Oregan. International distribution to Canada, Estonia, France, Germany, Japan, Netherlands, Spain, Switzerland, United Kingdom.
About Philips North America Llc
Philips North America Llc has 301 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report