FDA Medical devices recall ·
IntelliVue G7m Anesthesia Gas Module, Product Number 866173 recall
- Recall number
- Z-0007-2025
- Date
- (initiated January 18, 2023)
- Company / brand
- Philips North America Llc
222 Jacobs St, Cambridge, MA, United States - Category
- Medical devices › Class II
- Classification
- Class II
- Status
- Ongoing
- Units affected
- 8,449 devices
- Initiated by
- Voluntary: Firm initiated
Read the official FDA notice ↗
Product
IntelliVue G7m Anesthesia Gas Module, Product Number 866173
Why was it recalled?
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.
What should you do?
FDA enforcement reports do not list a consumer remedy. Check the product codes below against what you have; if it matches, stop using it and follow the instructions in the firm's or FDA's official notice, or contact the company. If you have health concerns, contact your healthcare provider.
Product codes & lot numbers
UDI-DI: 00884838051492; Serial Numbers: DE43800129 through DE43812627
Distribution
US Nationwide. Global Distribution.
What does Class II mean?
Class II means use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or the probability of serious harm is remote.
Source: FDA (medical devices), recall Z-0007-2025. Official notice. Republished from public data; RecallFlag is not affiliated with the FDA.