Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
SonarMed AirWave Monitor Kit (Monitor Recalled by Covidien, LP Due to Prior to use on a patient, the device...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Covidien, LP directly.
Affected Products
SonarMed AirWave Monitor Kit (Monitor, Sensor Cable, Power Cord), Item Code AW-M0001. used with endotracheal tube (ETT)
Quantity: 66 devices
Why Was This Recalled?
Prior to use on a patient, the device alarm speaker failed to annunciate on power up and the device falsely detected a sensor cable disconnect and reconnect during setup. The monitor detection of a false sensor cable disconnect and reconnect may cause the monitor to discontinue monitoring and transition into the calibration screen without an audible alarm.
Where Was This Sold?
This product was distributed to 9 states: CA, CO, FL, IL, KY, MA, OH, TN, TX
About Covidien, LP
Covidien, LP has 68 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report