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Open, Classified

IntelliVue G7m Anesthesia Gas Module, Product Number 866173

FDA Recall Z-0007-2025 · Posted 2024-10-01

Recalling FirmPhilips North America
Recall StatusOpen, Classified
Product CodeDSI
Date Initiated2023-01-18
Product Quantity8,449 devices

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.

Firm Action

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.

Root Cause

Under Investigation by firm

Distribution Pattern

US Nationwide. Global Distribution.

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

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