Serious health hazard — there is a reasonable probability that use of or exposure to this product will cause serious adverse health consequences or death.
AW-S025 NEO SONARMED SENSOR 2.5MM. Used in conjunction with SonarMed Recalled by SonarMed Inc Due to The failure to detect the partial obstruction in...
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 SonarMed Inc directly.
Affected Products
AW-S025 NEO SONARMED SENSOR 2.5MM. Used in conjunction with SonarMed Monitor for airway monitoring.
Quantity: 610 units
Why Was This Recalled?
The failure to detect the partial obstruction in a 2.5mm sensor.
Where Was This Sold?
This product was distributed to 19 states: AK, AZ, CA, FL, IL, KY, MD, MO, NJ, NY, NC, OH, OR, PA, SC, TN, TX, VA, WA
About SonarMed Inc
SonarMed Inc has 5 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report