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Philips North America, LLC recalls IntelliVue MX40 Patient Monitor, Product number 857146, Service Numbers All: 453564711531 and 453564711541 - Product Us
Recalled June 12, 2019 · FDA recall Z-1695-2019 · Philips North America
Hazard
The MX40 may experience increased power consumption and may have a lack of visual and/or audible notifications while in a Low Battery State . · FDA Class II
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Worldwide distribution - US Nationwide and to 71 countries.
Description
The MX40 may experience increased power consumption and may have a lack of visual and/or audible notifications while in a Low Battery State .
Product
IntelliVue MX40 Patient Monitor, Product number 857146, Service Numbers All: 453564711531 and 453564711541 - 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.
Manufacturer(s)
Philips North America, LLC
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →