FDA Device recall Z-0007-2025
IntelliVue G7m Anesthesia Gas Module, Product Number 866173
- FDA Device
- Class II
- ongoing
- Published 2024-10-09
On 2024-10-09 the FDA classified a Class II recall of IntelliVue G7m Anesthesia Gas Module, Product Number 866173 by Philips North America, citing 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 pum….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0007-2025 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2023-01-18 |
| Published | 2024-10-09 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | Philips North America |
| Distribution | US |
Product
IntelliVue G7m Anesthesia Gas Module, Product Number 866173
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.
Identifiers
| code_info | UDI-DI: 00884838051492; Serial Numbers: DE43800129 through DE43812627 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:57 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0007-2025%22
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