SonarMed recalls its AW-S025 NEO Sonarmed Sensor 2.5mm airway monitoring device due to potential failure to detect partial obstructions in airways.
The failure to detect the partial obstruction in a 2.5mm sensor.
SonarMed is recalling its AW-S025 NEO Sonarmed Sensor 2.5mm airway monitoring sensor because it may fail to detect partial obstructions in the airway. This could lead to serious health risks if the sensor is used without proper detection.
The sensor may fail to detect partial obstructions in the airway, which can lead to serious health issues if the obstruction is not identified. This risk is specific to the airway monitoring context where timely detection is critical.
Healthcare providers using this sensor for airway monitoring are most at risk. Patients relying on this device for airway monitoring could experience undetected obstructions.
Check for the product serial numbers listed: A20221012, A20221018, A20221025, A20221107, A20221109, A20221202, A20221206, A20221207, A20221208, A20221209, A20230105, A20230109, A20230123, A20230124, A20230125, A20230126, A20230213, A20230224, A20230228, A20230301, A20230302, A20230303, A20230320, A20230324, A20230411, A20230724, A20230725.
Look for the product serial numbers listed in the recall notice: A20221012, A20221018, A20221025, A20221107, A20221109, A20221202, A20221206, A20221207, A20221208, A20221209, A20230105, A20230109, A20230123, A20230124, A20230125, A20230126, A20230213, A20230224, A20230228, A20230301, A20230302, A20230303, A20230320, A20230324, A20230411, A20230724, A20230725.
The sensor may fail to detect partial obstructions in the airway, which could lead to serious health risks if the obstruction is not identified.
Check if your sensor has a serial number listed in the recall notice. If it does, stop using it and contact SonarMed for further instructions.
The recall record does not mention a remedy or fix for this issue.
We’ve drafted a message you can send SonarMed to request your refund or repair — edit it as you like.
Subject: Recall Z-1519-2024 — SonarMed SonarMed Hello, I own a SonarMed that is covered by recall Z-1519-2024 from SonarMed. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
