--- title: "SonarMed Inc Recalls: Agency-Reported Status and History (Oct 1, 2026) | Is It on Recall" description: "Search SonarMed Inc recall records, lots, firms and dates. Reported status can be incomplete; use the linked agency notice for current instructions." url: https://isitonrecall.com/brand/sonarmed-inc/ updated: 2026-10-01 site: "Is It on Recall" language: en --- [Home](https://isitonrecall.com/) / Brand archive # SonarMed Inc recall records **4** reported ongoing 4 records in this archive. Latest source date Mar 25, 2024. FDA enforcement status can lag behind the recall lifecycle. An empty search or a reported termination is not a personal product-safety determination. Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/). ## Records and reported status Mar 25, 2024 FDA device enforcement ### [AW-M0001 SONARMED MONITOR. Used in conjunction with SonarMed Acoustic Sensors for airway monitoring.](https://isitonrecall.com/recall/fda-device-z-1535-2024-aw-m0001-sonarmed-monitor-used-in-conjunction-with-sonarmed-acoustic-sensors-for-airway-monitoring/) Software anomaly resulted in failure to detect a partial obstruction in 2.5 mm sensors and up to 3mm distal to the sensor. Class I Reported ongoing Distribution: \_AK, AZ, CA, FL, IL, KY, MD, MO, NC, NJ, NY, OH, OR, PA, SC, TN, TX, VA, & WA\_ [Official source for AW-M0001 SONARMED MONITOR. Used in conjunction with SonarMed Acoustic Sensors for airway monitoring.](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1535-2024%22) Mar 21, 2024 FDA device enforcement ### [AW-S025 NEO SONARMED SENSOR 2.5MM. Used in conjunction with SonarMed Monitor for airway monitoring.](https://isitonrecall.com/recall/fda-device-z-1519-2024-aw-s025-neo-sonarmed-sensor-2-5mm-used-in-conjunction-with-sonarmed-monitor-for-airway-monitoring/) The failure to detect the partial obstruction in a 2.5mm sensor. Class I Reported ongoing Distribution: Domestic: AK, AZ, CA, FL, IL, KY, MD, MO, NC, NJ, NY, OH, OR, PA, SC, TN, TX, VA, & WA. [Official source for AW-S025 NEO SONARMED SENSOR 2.5MM. Used in conjunction with SonarMed Monitor for airway monitoring.](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1519-2024%22) Mar 21, 2024 FDA device enforcement ### [AW-S030 NEO SONARMED SENSOR 3.0MM. Used in conjunction with SonarMed Monitor for airway monitoring.](https://isitonrecall.com/recall/fda-device-z-1520-2024-aw-s030-neo-sonarmed-sensor-3-0mm-used-in-conjunction-with-sonarmed-monitor-for-airway-monitoring/) The failure to detect the partial obstruction in a 2.5mm sensor. Class I Reported ongoing Distribution: Domestic: AK, AZ, CA, FL, IL, KY, MD, MO, NC, NJ, NY, OH, OR, PA, SC, TN, TX, VA, & WA. [Official source for AW-S030 NEO SONARMED SENSOR 3.0MM. Used in conjunction with SonarMed Monitor for airway monitoring.](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1520-2024%22) Mar 21, 2024 FDA device enforcement ### [AW-S035 NEO SONARMED SENSOR 3.5MM. Used in conjunction with SonarMed Monitor for airway monitoring.](https://isitonrecall.com/recall/fda-device-z-1521-2024-aw-s035-neo-sonarmed-sensor-3-5mm-used-in-conjunction-with-sonarmed-monitor-for-airway-monitoring/) The failure to detect the partial obstruction in a 2.5mm sensor. Class I Reported ongoing Distribution: Domestic: AK, AZ, CA, FL, IL, KY, MD, MO, NC, NJ, NY, OH, OR, PA, SC, TN, TX, VA, & WA. [Official source for AW-S035 NEO SONARMED SENSOR 3.5MM. Used in conjunction with SonarMed Monitor for airway monitoring.](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1521-2024%22) ## Reasons in these listed records - Software anomaly resulted in failure to detect a partial obstruction in 2.5 mm sensors and up to 3mm distal to the sensor. - The failure to detect the partial obstruction in a 2.5mm sensor. These examples come from this result page and are not a ranking of every recall reason. ## Checking SonarMed Inc ### Is there a recall on sonarmed inc right now? This archive contains 4 records, including 4 with agency-reported ongoing status. The status field can be incomplete or stale. Open the current official notice and match your exact product. ### How do I check my package or product? Compare the product, firm and lot, date, model or serial identifiers with the notice. [Use the label-check guide](https://isitonrecall.com/guides/read-lot-codes/) if you need help locating an identifier. ### Does a matching name mean every item is included? A name is a search match. The agency notice sets the affected products and identifiers. Do not assume that every item with the same name or brand belongs to the recall. ### What if the search finds no matching record? This search has source and keyword limits. Missing records or a missing lot code do not establish that a product is unaffected. [Check source coverage](https://isitonrecall.com/sources/) and the agency's current notices. ### Where can I find older records? Use [monthly archives](https://isitonrecall.com/archives/) or the local search. The initial import covers records dated from October 2021 where available; each source's actual first and latest dates appear on the coverage page. ## Keep checking [Search SonarMed Inc](https://isitonrecall.com/check/?q=SonarMed%20Inc) [Browse related products](https://isitonrecall.com/products/) [Review source dates](https://isitonrecall.com/sources/)