IntelliVue G7m Anesthesia Gas Module — Class II medical device recall Z-0007-2025
Ongoing recall by Philips North America, reported 2024-10-09, distributed nationwide. The 866173 lntelliVue G7m Anesthesia Gas Modules could have a component issue that may trigger an interruption
| Recall number | Z-0007-2025 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Philips North America, Cambridge, MA, United States |
| Recall initiated | 2023-01-18 |
| Classified | 2024-10-01 |
| Reported by FDA | 2024-10-09 |
| Distributed | Nationwide (US) |
| Quantity | 8,449 devices |
| Reason classes | device malfunction |
| UPC / GTIN / UDI-DI | 00884838051492 |
| Serial numbers | DE43800129 |
Product
IntelliVue G7m Anesthesia Gas Module, Product Number 866173
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0007-2025. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.