# FDA recall Z-1693-2019

> **Philips North  America, LLC** · Class II · device recall initiated 2019-03-28.

## Product

IntelliVue MX40 Patient Monitor, Product number 865351, Service Numbers  All other countries: 453564451791, 453564451811, 453564467721, 453564467741, 453564467761, 453564467781, 453564467801, 453564467821, 453564467841, 453564467861, 453564262531, and 453564262551 - Product Usage: Used primarily as a traditional telemetry medical device. It connects to the IntelliVue Information Center by way of a wireless network. When the MX40 is connected to the IntelliVue Information Center the IntelliVue Information Center provides the primary patient monitoring and alarming function. The MX40 does not automatically provide local monitoring or alarming when connected to the Information Center.

## Reason for recall

The MX40 may experience increased power consumption and may have a lack of visual and/or audible notifications while in a  Low Battery State .

## Distribution

Worldwide distribution - US Nationwide and to 71 countries.

## Key facts

- **Recall number:** Z-1693-2019
- **Recalling firm:** Philips North  America, LLC
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2019-03-28
- **Report date:** 2019-06-12

- **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-1693-2019

## Citation

> AI Analytics. FDA recall Z-1693-2019. Retrieved 2026-06-02 from https://api.ai-analytics.org/recall/Z-1693-2019. Source: US FDA. Licensed CC0.

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