FDA Medical Device Recalls (openFDA)
Philips North America: IntelliVue G7m Anesthesia Gas Module, Product Number 866173
- Recall number
- Z-0007-2025
- Recalling firm
- Philips North America
- Product
- IntelliVue G7m Anesthesia Gas Module, Product Number 866173
- Status
- Open, Classified
- Initiated
- 2023-01-18
- Posted
- 2024-10-01
- Terminated
- not on file
- Reason
- 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.
- Root cause
- Under Investigation by 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.
- Quantity
- 8,449 devices
- Distribution
- US Nationwide. Global Distribution.
- Lot, serial or model codes
- UDI-DI: 00884838051492; Serial Numbers: DE43800129 through DE43812627
- 510(k) numbers
- ["K151681"]
- PMA numbers
- not on file
- Product code
- DSI
- Firm FEI
- 3006648320
- Firm city
- Cambridge
- Firm state
- MA
- Firm country
- not on file
Where this comes from
- Register
- FDA Medical Device Recalls (openFDA)
- Publisher
- U.S. Food and Drug Administration (openFDA)
- File
- device-recall-0001-of-0001.json.zip
- sha256
- b87518bfe2e8
- Size
- 288210821 bytes
- Published
- 2026-09-28
- Read
- 2026-09-29T08:25:23.626Z
- Source file
- Source file retained · verify
- Refresh due
- 2026-10-06
Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.
Cite as
FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28