# FDA recall Z-2689-2020

> **Philips North  America, LLC** · Class II · device recall initiated 2020-06-25.

## Product

IntelliVue G7m Anesthesia Gas Module, Model no. 866173, Firmware Version 04.12.00, System Codes 453564477391, 453564477401, 866173

## Reason for recall

The device may experience an interruption of gas measurement due to a firmware issue, ceasing measurement and display of gas levels and generating one or more technical or INOP alarms.

## Distribution

Worldwide distribution - US Nationwide distribution.

## Key facts

- **Recall number:** Z-2689-2020
- **Recalling firm:** Philips North  America, LLC
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2020-06-25
- **Report date:** 2020-07-29

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Andover, MA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2689-2020

## Citation

> AI Analytics. FDA recall Z-2689-2020. Retrieved 2026-07-15 from https://api.ai-analytics.org/recall/Z-2689-2020. Source: US FDA. Licensed CC0.

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