Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-1520-2024 — AW-S030 NEO SONARMED SENSOR 3.0MM. Used in conjunction with SonarMed Monitor for airway monitoring.

U.S. FDA — Device Enforcement · United States · 2024-03-21 · Class I

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1520-2024
Date of alert
2024-03-21
Country / jurisdiction
United States
Risk level
Class I
Risk type
recall
Brand
SonarMed Inc
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
10851334007190
Reported risk: The failure to detect the partial obstruction in a 2.5mm sensor.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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