Medical Device Recall: IntelliVue G7m Anesthesia Gas Module, Product Number 866173
Philips North America · January 18, 2023
Reason for Recall
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.
Distribution
US Nationwide. Global Distribution.
States Affected
NATIONWIDE
Quantity Affected
8,449 devices
Source: FDA (openFDA Device Enforcement)
Recall number: Z-0007-2025
Status: ongoing
SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.