Use cautionMedical device recall · FDA · Published January 18, 2023
Philips IntelliVue G7m Anesthesia Gas Module Recall: Gas Measurement Interruption Risk
Philips recalls IntelliVue G7m Anesthesia Gas Module (Product 866173) due to potential gas measurement interruption from a sample pump issue. Affected units may trigger inoperable alarms.
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.
Take action
Contact the company
📍Recalling firmPhilips North America222 Jacobs St · Cambridge, MA 02141-2296
“Philips IntelliVue G7m Anesthesia Gas Module Recall: Gas Measurement Interruption Risk.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/59028-philips-intellivue-g7m-anesthesia-gas-module-recall-gas-measurement-interruption. Based on FDA recall #Z-0007-2025 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0007-2025%22&limit=1).
The FDA announced on Jan. 18, 2023, that Philips North America is recalling the IntelliVue G7m Anesthesia Gas Module (Product Number 866173) due to a component issue that may interrupt gas measurement. The company issued an Important Product Notice regarding the recall.
How to tell if you have it
Brand: Philips
Product: IntelliVue G7m Anesthesia Gas Module
Product Number: 866173
UDI-DI: 00884838051492
Serial Numbers: DE43800129 through DE43812627
The hazard
The G7m's sample gas pump could stop working due to friction caused by abrasion, producing a technical INOP (inoperable) alarm. This issue concerns the module's ability to measure gas correctly.
Context
GovInfoNow's records show Philips North America has 30 other recalls on record since Dec. 24, 2020. Other recent recalls of similar products include Datex-Ohmeda Aisys Anesthesia System Recall (July 30, 2026), Draeger Vapor 3000 Anesthetic Vaporizer Recall (Nov. 24, 2025), and Datex-Ohmeda Aisys CS2 Anesthesia System Recall (July 30, 2026).
How to tell if you have this one
Check for Product Number 866173 on the module. Affected units have serial numbers from DE43800129 to DE43812627 and were sold in the U.S. starting from the IMPORTANT PRODUCT NOTICE date of January 18, 2023.
Brand
Philips
Category
Medical device
Based on the official FDA remedy
What to do — step by step
Check Module Status
Verify if the module triggers an inoperable alarm when the gas pump stops working.
Where it went and when
Where it was distributed
Distributed nationwide.
Nationwide
Not listed
FDA distribution: “US Nationwide. Global Distribution.” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide.
Recall timeline
FDA published this recall 21 months after the firm started it.
1Firm started the recall
2FDA classified it Class II
3Published in FDA’s Enforcement Report
Dates from the agency record only; steps without a date are left out.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
Official source: FDA Recall #Z-0007-2025 (January 18, 2023) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0007-2025 to see it in context.
Plain-language summary written by qwen3:4b on August 19, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.