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Philips Electronics North America Corporation recalls IntelliVue Multi Measurement Server, IntelliVue Multi Measurement Server SLCP, IntelliVue Multi Measurement Server X2, I
Recalled January 3, 2018 · FDA recall Z-0292-2018 · Philips Electronics North America
Hazard
Distorted ST-Segment when using 12-Lead ECG Monitoring with Philips IntelliVue Patient Monitors · FDA Class II
Units
7071
Sold at
Worldwide Distribution and US Nationwide
Description
Distorted ST-Segment when using 12-Lead ECG Monitoring with Philips IntelliVue Patient Monitors
Product
IntelliVue Multi Measurement Server, IntelliVue Multi Measurement Server SLCP, IntelliVue Multi Measurement Server X2, IntelliVue Patient Monitor Models MP2 and MP5 Product Usage: Indicated for use by health care professionals whenever there is a need for monitoring the physiological parameters of patients. Intended for monitoring, recording, and alarming of multiple physiological parameters of adults, pediatrics, and neonates in a hospital environment.
Manufacturer(s)
Philips Electronics North America Corporation
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →