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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 Airway monitors recalled for a software issue where it fails to detect partial obstructions in 2.5mm sensors and within 3mm of sensor tip.

http://www.fda.gov/medical-devices/medical-device-recalls/sonarmed-inc-recalls-airway-monitors-due-software-anomaly-resulting-failure-detect-partial

 
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SonarMed Inc. Recalls Airway Acoustic Sensors Due to a Restricted Inner Diameter of Airway Causing Suction Catheter Passage Difficulty

SonarMed Airway acoustic sensors recalled due to a restricted inner diameter resulting in difficulty passing a suction catheter through the sensor.

http://www.fda.gov/medical-devices/medical-device-recalls/sonarmed-inc-recalls-airway-acoustic-sensors-due-restricted-inner-diameter-airway-causing-suction