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SonarMed Inc recalls SonarMed AirWave Monitor, Model Number M0001
Recalled September 11, 2019 · FDA recall Z-2450-2019 · SonarMed
Hazard
Potential for the presence of two error codes which would make the monitor inoperable. · FDA Class II
Units
16 units
Sold at
CA & TX
Description
Potential for the presence of two error codes which would make the monitor inoperable.
Product
SonarMed AirWave Monitor, Model Number M0001
Manufacturer(s)
SonarMed Inc
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →