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Medrad Mr Inc recalls Medrad Veris MR Monitor units The system is intended to monitor physiological parameters of patients within any heal
Recalled January 29, 2014 · FDA recall Z-0810-2014 · Medrad Mr
Hazard
The main board, P/N 301641, installed in some Medrad Veris MR Monitor units may be faulty and could lead to unexpected shutdown of the system while in use, resulting in the loss of vital signs information from the monitor. · FDA Class II
Units
922 units
Sold at
Worldwide Distribution: US (nationwide) and Internationally to: Canada.
Description
The main board, P/N 301641, installed in some Medrad Veris MR Monitor units may be faulty and could lead to unexpected shutdown of the system while in use, resulting in the loss of vital signs information from the monitor.
Product
Medrad Veris MR Monitor units The system is intended to monitor physiological parameters of patients within any healthcare environment. The user, responsible to interpret the monitored data made available, will be a professional healthcare provider. Physiological data, gas monitoring, system alarms, and patient analysis will be available to the care provider from the monitor.
Manufacturer(s)
Medrad Mr Inc
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →