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Invivo Corporation recalls Philips Expression MR200 MRI Patient Monitoring System
Recalled October 22, 2014 · FDA recall Z-0069-2015 · Invivo
Hazard
Failure to produce the Non-Invasive Blood Pressure (NIBP) Measurement. · FDA Class II
Units
24 units.
Sold at
Worldwide Distribution - US including the states of CA, GA, MI, NJ, NV, and TX., and the countries of: Austria, Finland, Germany, Poland, Singapore, Sweden, Switzerland and United Kingdom.
Description
Failure to produce the Non-Invasive Blood Pressure (NIBP) Measurement.
Product
Philips Expression MR200 MRI Patient Monitoring System
Manufacturer(s)
Invivo Corporation
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →