Philips North America IntelliVue G7m Anesthesia Gas Module, Product Number 866173 Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
IntelliVue G7m Anesthesia Gas Module, Product Number 866173
Brand
Philips North America
Lot Codes / Batch Numbers
UDI-DI: 00884838051492, Serial Numbers: DE43800129 through DE43812627
Products Sold
UDI-DI: 00884838051492; Serial Numbers: DE43800129 through DE43812627
Philips North America is recalling IntelliVue G7m Anesthesia Gas Module, Product Number 866173 due to The 866173 lntelliVue G7m Anesthesia Gas Modules could have a component issue that may trigger an interruption of the gas measurement. This issue conc. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
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.
Recommended Action
Per FDA guidance
An IMPORTANT PRODUCT NOTICE dated 1/18/23 was sent to customers. The actions planned by Philips to correct the problem A Philips representative will reach out to you to arrange a replacement of the sample gas pump. Affected products and how to identify them Affected product is the 866173 lntelliVue G7m Anesthesia Gas Module. Both the product number and the serial number on the G7m product is contained on the back of the product, preceded by "REF" and "SN", respectively. If you need any further information or support concerning this issue, please contact your local Philips representative.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026