SonarMed AirWave AW-S025Recalls & reported problems
Sonarmed, Inc · Neonatal SonarMed Sensor - for use with endotracheal tubes of 2.5 mm ID · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
1 open recall names this device. See the recall details and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 0
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 1
Summary
No MAUDE adverse event reports in our data reference this device identifier directly.
1 FDA recall record name this device's identifier, 1 still open.
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.
Recalls naming this device
- Mar 21, 2024Class IOpen, Classified
The failure to detect the partial obstruction in a 2.5mm sensor.
Z-1519-2024 · Root cause: Process control · Recall details · FDA record ↗
Other Airway Monitoring System devices
- SonarMed AirWave AW-M0001Sonarmed, Inc · Airway Monitoring System3 recalls2 reports
- SonarMed AirWave AW-S030Sonarmed, Inc · Airway Monitoring System1 recall3 reports
- SonarMed AirWave AW-S035Sonarmed, Inc · Airway Monitoring System1 recall1 report
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026 · each recall links to the FDA recall notice
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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