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https://prais.paho.org/en/sonarmed-inc-recalls-airway-monitors-due-to-a-software-anomaly-resulting-in-failure-to-detect-a-partial-obstruction-in-2-5mm-sensors-and-up-to-3mm-distal-to-the-sensor-tip/ SonarMed Inc. Recalls Airway Monitors Due to a Software Anomaly Resulting in Failure to Detect a... https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfRes/res.cfm?ID=206852 Class 1 Device Recall SonarMed AirWave class device recall airwave https://www.fda.gov/medical-devices/medical-device-recalls-and-early-alerts/sonarmed-inc-recalls-airway-monitors-due-software-anomaly-resulting-failure-detect-partial SonarMed Inc. Recalls Airway Monitors Due to a Software Anomaly Resulting in Failure to Detect a... SonarMed Airway monitors recalled for a software issue where it fails to detect partial obstructions in 2.5mm sensors and within 3mm of sensor tip.