Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
IntelliVue G7m Anesthesia Gas Module Recalled by Philips North America Due to The 866173 lntelliVue G7m Anesthesia Gas Modules could...
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
IntelliVue G7m Anesthesia Gas Module, Product Number 866173
Quantity: 8,449 devices
Why Was This Recalled?
The 866173 lntelliVue G7m Anesthesia Gas Modules could have a component issue that may trigger an interruption of the gas measurement. This issue concerns the G7m's sample gas pump which could stop working, producing a technical, INOP (inoperable) alarm. The pump may fail prematurely when there is friction caused by an abrasion. This recall is for an IMPORTANT PRODUCT NOTICE dated 1/18/23.
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